TW460518B - Preparing process of cellular thermoplastic polymer foam and manufactured products thereof, and foam suitable for use therein - Google Patents

Preparing process of cellular thermoplastic polymer foam and manufactured products thereof, and foam suitable for use therein Download PDF

Info

Publication number
TW460518B
TW460518B TW088108888A TW88108888A TW460518B TW 460518 B TW460518 B TW 460518B TW 088108888 A TW088108888 A TW 088108888A TW 88108888 A TW88108888 A TW 88108888A TW 460518 B TW460518 B TW 460518B
Authority
TW
Taiwan
Prior art keywords
foam
scope
patent application
thermoplastic polymer
item
Prior art date
Application number
TW088108888A
Other languages
Chinese (zh)
Inventor
Chung P Park
Original Assignee
Dow Chemical Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dow Chemical Co filed Critical Dow Chemical Co
Application granted granted Critical
Publication of TW460518B publication Critical patent/TW460518B/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/36After-treatment
    • C08J9/38Destruction of cell membranes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34Auxiliary operations
    • B29C44/56After-treatment of articles, e.g. for altering the shape
    • B29C44/5627After-treatment of articles, e.g. for altering the shape by mechanical deformation, e.g. crushing, embossing, stretching
    • B29C44/5663After-treatment of articles, e.g. for altering the shape by mechanical deformation, e.g. crushing, embossing, stretching by perforating the foam, e.g. to open the cells

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Cell Biology (AREA)
  • Mechanical Engineering (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • External Artificial Organs (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Soundproofing, Sound Blocking, And Sound Damping (AREA)
  • Peptides Or Proteins (AREA)
  • Extraction Or Liquid Replacement (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Thermoplastic polymer foams having sound deadening properties satisfactory for demanding applications are provided which have mechanical strength, which are economical to manufacture, and which are hydrolytically stable. Methods of preparing these foams are also provided. The foams are useful in sound management, cushion packaging, filtering, and fluid absorption and exhibit one or more of the following properties: (1) average cell size greater than about 2 mm; (2) substantially open cell structure and (3) relatively large pores connecting the cells. In order that the foam be acoustically active, the foam should posses a substantially open cell structure and a relatively low airflow resistivity. Foams with substantially open cell structure and relatively low airflow resistivity are prepared by mechanically opening a foam having an average cell size greater than about 2 mm. In most cases, such mechanical opening creates relatively large pores connecting the cells.

Description

460518 A7 _____B7_ 五、發明説明(1 ) 本發明大體而言係有關於發泡體,且更詳言之係有關 於可使用在聲音管理上之熱塑性聚合物發泡體。 在建築工業中使用鎮板作為分隔牆俾將建築區域分成 分開的區域諸如房間或辦公室為習知者。通常它們由一絕 緣礦物纖維核心與包圍核心的二外側覆面層以及一氣陳或 中空間隔所組成。絕緣材料諸如礦物纖維係以一提供熱及 /或聲音隔絕之方式配置於覆面層之間。但是,此種具有 纖維核心之隔板或讓板的一大缺點為此種纖維缺少機械強 度因此需要一高價之支持構造或敏密化。此外,礦物纖維 產品處理麻煩’造成皮膚刺激且可能呈現對健康的危險。 發泡體亦已被利用作為聲音隔絕材料。例如,w〇 95 / 1413 6揭露多層絕緣板或元件’在一較佳實施例中包括(a) 二外側覆面層’以及(b) —軟合成核心材料,其為一具有 中空剖面之單一、連續、軟、合成、閉合胞室發泡體核心 層。此核心材料被安排成透過交錯圖案之接觸點與兩外層 密切接觸,俾在核心層與相對外層之間提供間隙。但是, 在W095 / 14136中被利用作核心層之閉合胞室發泡體對 於需要之應用的隔音不盡令人滿意。 經濟部中央標丰局貝工消費合作社印聚 (請先閲讀背面之注意事項再填寫本頁) 雖然不希望被任何特殊理論拘限,本案發明人相信 聲音管理(例如吸音和隔音)用之一特殊聚合物發泡體的 效用係視具有下述性質之發泡體而定:1 )平均大於約2mm 之胞室大小;2)大體上敞開胞室構造以及3)比較大的連 接胞室孔隙。為了使發泡體能以感音,發泡體應具有一實 質上敞開胞室構造與一比較低的氣流阻力。同時亦相信這 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 4 4 6051 8 A7 B7 五、發明説明(2 經濟部中央標準局員工消費合作社印製 些性質中的一項或一項以上造成一發泡體對過濾和流體吸 收之效用。 某些大氣孔、敞開胞室之發泡體係為習知者。但是 ’它們亦具有一些缺點。例如,熱固性樹脂諸如蜜胺以及 半固聚氨酯可被用來製備發泡體,此種發泡體展現相信係 為聲音管理所需要的理想大氣孔、敞開胞室構造。但是, 熱固性樹脂係不能回收者,製造成本高且由於其水解不穩 定性而不適於使用在潮濕或多雨的環境中。熱塑性聚合物 發泡體一般而言係藉由一合宜的擠壓程序廉價地製造,為 可回收者’且展現水解穩定性,因此提供凌越熱固性樹脂 之優點。但是,藉由一合宜的直接擠壓程序達成一具有敞 開胞室構造之大氣孔熱塑性發泡體卻有困難。此一困難存 在之原因在於胞室敞開與發泡體膨脹彼此對立。亦即,在 發泡體内成長之胞室必須保持閉合俾能成長,但發展成一 大氣孔則需要在發泡結束之前短時間内在胞室壁上產生一 孔洞。 此外,雖然某些熱塑性聚合物發泡體據言在聲音管 理上有其效用,其聲音管理性能在一需要之應用場合中是 否令人滿意則存疑。(參見例如1988,2, 1 1日公告,Dynamit Nobel AG名下之DE 3626349,1988,2,11 公告,Dynamit Nobel AG名下之DE 3626350,以及 1995,5,26公告,Dow Chemical名下之WO 95/14136)。 因此,業界冀求對於需要之應用上提供令人滿意之 隔聲性質的發泡體,該等發泡體具有機械強度,製造經濟 --·--^-----澤-- (請先閱讀背面之注意事項再填寫本頁) t -β Γ460518 A7 _____B7_ V. Description of the invention (1) The present invention generally relates to a foam, and more specifically, to a thermoplastic polymer foam that can be used for sound management. In the construction industry, a townboard is used as a partition wall. Dividing a building area into separate areas such as rooms or offices is known. They usually consist of an insulated mineral fiber core, two outer cladding layers surrounding the core, and an aged or hollow space. Insulating materials such as mineral fibers are disposed between the facing layers in a manner that provides thermal and / or sound insulation. However, a major disadvantage of such a separator having a fiber core or a board is that the fiber lacks mechanical strength and therefore requires a high-priced support structure or densification. In addition, the processing trouble of mineral fiber products' causes skin irritation and may present a danger to health. Foams have also been used as sound insulation materials. For example, WO95 / 11413 discloses that a multilayer insulation board or element 'includes (a) two outer facing layers' and (b) a soft synthetic core material in a preferred embodiment, which is a single, Continuous, soft, synthetic, closed cell foam core layer. The core material is arranged to make close contact with the two outer layers through the contact points of the staggered pattern, and to provide a gap between the core layer and the opposite outer layer. However, the closed cell foam used as the core layer in W095 / 14136 is not satisfactory for the sound insulation of required applications. Printed by the Biaofeng Consumer Cooperative of the Central Biaofeng Bureau of the Ministry of Economic Affairs (please read the notes on the back before filling this page). Although not wishing to be bound by any special theory, the inventor of this case believes that one of the sound management (such as sound absorption and sound insulation) is used The effectiveness of the special polymer foam depends on the foam having the following properties: 1) the cell size is on average greater than about 2mm; 2) the structure of the cell is generally open; and 3) the cell pores are relatively large . In order to make the foam sound sensitive, the foam should have a substantially open cell structure and a relatively low airflow resistance. At the same time, I believe that this paper size is applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm) 4 4 6051 8 A7 B7 V. Description of the invention (2 One of the properties printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs or More than one cause the effectiveness of a foam for filtration and fluid absorption. Certain atmospheric cells and open cell foam systems are known. But 'they also have some disadvantages. For example, thermosetting resins such as melamine and Polyurethane can be used to prepare foams. Such foams are believed to be ideal for air management and have open cell structures. However, thermoset resins cannot be recycled, which is costly to manufacture and due to their hydrolysis. Unstable for use in wet or rainy environments. Thermoplastic polymer foams are generally manufactured inexpensively through a suitable extrusion process, are recyclable 'and exhibit hydrolytic stability, thus providing The advantages of Ling Yue thermosetting resin. However, an open-cell thermoplastic foam with an open cell structure is achieved by a suitable direct extrusion process There is a difficulty. The reason for this difficulty is that the open cells and the expansion of the foam oppose each other. That is, the cells that grow in the foam must be kept closed to grow, but the development of an air cell requires foaming. A hole was created in the cell wall shortly before the end. In addition, although some thermoplastic polymer foams are said to have utility in sound management, whether their sound management performance is satisfactory in a required application Doubtful. (See, for example, the Announcement on February 11, 1988, DE 3626349 under the name of Dynamit Nobel AG, Announcement on February 2, 11, 1988, DE 3626350 under the name of Dynamit Nobel AG, and the Announcement on May 5, 26, 1995. The following WO 95/14136). Therefore, the industry desires to provide foams with satisfactory sound insulation properties for applications where they are needed. These foams have mechanical strength and are economical to manufacture ----- ^- --- Ze-- (Please read the notes on the back before filling in this page) t -β Γ

I 本紙張尺度適用中國國家標準(CNS ) Α4規格(210X297公釐) 5 46051 8 A7 __ ____B7 五、發明說明(斗) 且水解穩定。 此一需求可被本發明滿足。因此,本發明提供在需 求用途上具有令人滿意之隔聲性質的熱塑性聚合物發泡 體,其具有機械強度,製造經濟且水解穩定。 於是,在本發明之一實施例中’提供具有大於約4mtn 之平均胞室尺寸的熱塑性聚合物發泡體。 在另一實施例中,具有大於約2mm之平均胞室大小 而其中50%以上之胞室已藉機械設備敞開的熱塑性聚合 物發泡體被提供》 在又一實施例令,本發明提供一熱塑性聚合物發泡體, 其具有低於約800000 Rays/m之氣流阻力以及大於2mm左右 之胞室大小’且其中50%以上的胞室已藉機械設備敞開, 在又另一實施例中,本發明提供製備熱塑性聚合物 發泡體構造之方法,該發泡體構造具有一大於約2mm之平 均胞室大小’且其中50%以上的胞室已藉機械設備敞開。 本發明之發泡體特別可用於聲音吸收、聲音隔絕、 流體吸收、過濾、緩衝包裝以及其他需要下列性質之應用 場合:聲音減弱或聲音阻尼性質、機械強度、經濟製造, 以及水解穩定性。 圖式簡要說明 第1圖繪示製備本發明之一發泡體的方法,其中在 一發泡體内之閉合胞室係藉穿孔敞開。 第2圖緣示製備本發明一發泡體之方法,其中在一 發泡體内之長形閉合胞室係藉穿孔敞開。 本紙張尺度適用t國國家標準(CNS>A4規格(210 «297公爱)----* -» — (靖先閱讀背面之注意事項再填寫本頁) 裝--------訂---------線 經濟部智慧財產局員工消費合作钍印制农 d60518 經濟部中央標準局員工消費合作社印製 A7 B7 五、發明説明(4 ) 第3圖繪示製備本發明一發泡體之方法,其中在一發 泡體内之長形閉合胞室係藉以一斜角穿孔敞開。 第4圖繪示一製備本發明發泡體之方法,其中在一發 泡體内之閉合胞室係藉隨於穿孔之後之壓縮被敞開。 第5圖繪示本發明一發泡體之聲音吸收曲線。 第6圖繪示本發明一發泡體之聲音吸收曲線。 第7圖繪示本發明一發泡體之聲音吸收曲線。 第8圖繪示本發明一發泡體之聲音吸收曲線。I The paper size applies to the Chinese National Standard (CNS) A4 specification (210X297 mm) 5 46051 8 A7 __ ____B7 5. Description of the invention (bucket) and stable hydrolysis. This need can be met by the present invention. Therefore, the present invention provides a thermoplastic polymer foam having satisfactory sound insulation properties in demanding applications, which has mechanical strength, is economical to manufacture, and is hydrolytically stable. Thus, in one embodiment of the present invention, ' a thermoplastic polymer foam having an average cell size greater than about 4mtn is provided. In another embodiment, a thermoplastic polymer foam having an average cell size greater than about 2 mm and more than 50% of which has been opened by mechanical equipment is provided. In another embodiment, the present invention provides a A thermoplastic polymer foam having an airflow resistance of less than about 800,000 Rays / m and a cell size greater than about 2 mm ', and more than 50% of the cells have been opened by mechanical equipment. In yet another embodiment, The invention provides a method for preparing a thermoplastic polymer foam structure having an average cell size greater than about 2 mm 'and more than 50% of which have been opened by mechanical equipment. The foam of the present invention is particularly useful for sound absorption, sound insulation, fluid absorption, filtration, cushioning packaging, and other applications requiring the following properties: sound attenuating or sound damping properties, mechanical strength, economical manufacturing, and hydrolytic stability. Brief Description of the Drawings Figure 1 illustrates a method for preparing a foamed body of the present invention, in which closed cells in a foamed body are opened by perforations. Fig. 2 shows a method for preparing a foamed body of the present invention, in which a long closed cell in a foamed body is opened by perforation. This paper size applies to national standards (CNS > A4 specifications (210 «297 public love) ---- *-» — (Jing first read the precautions on the back before filling out this page) Loading -------- Order --------- Online consumer cooperation between the Intellectual Property Bureau of the Ministry of Economic Affairs and printed agriculture d60518 Printed on the A7 B7 by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs 5. Description of the invention (4) Figure 3 shows the preparation of this A method of inventing a foam, wherein the elongated closed cell in a foam is opened by an oblique perforation. Fig. 4 illustrates a method for preparing the foam of the present invention, in which a foam The closed cell inside is opened by compression after perforation. Figure 5 shows the sound absorption curve of a foam of the present invention. Figure 6 shows the sound absorption curve of a foam of the present invention. Section 7 The figure shows the sound absorption curve of a foam of the present invention. Figure 8 shows the sound absorption curve of a foam of the present invention.

第9圖鳍'示本發明一發泡艘之剖面,該剖面被標示為 I 第1 〇圖繪示本發明一發泡體之剖面,該剖面被標示 為U。 第11圖緣示本發明一發泡體之剖面,該剖面被標示 為W。 本發明提供一具有滿足需要應用之隔音性質的熱塑 性聚合物發泡體,該發泡體具有機械強度,可經濟地製造 且為水解穩定者。本發明之發泡體展現了迄今難以達成一 即便非不可能達成之諸性質組合。因此,本發明之發泡體 展現以下性質的一種或一種以上:1 )大於2mm左右之平 均胞室大小;2 )大體上敞開胞室構造以及3 )比較大的連 接胞室之孔隙。為了使得發泡體有效感音,發泡體應具有 一大體上敞開胞室之構造以及一比較低的氣流阻力。依據 本發明’具有大體上敞開胞室構造與比較低之氣流阻力的 發泡體係由機械地敞開具一大於2mm左右之平均胞室尺寸 本紙張尺度適用中國國家標车(CNS ) Α4規格(210 X 2?7公釐) I I - - ί I - - -- -1 (請先閱讀背面之注意事項再填寫本頁) 4 6051 8 A7 B7 經濟部中央標準局員工消費合作社印製 五、發明説明(5 的發泡體而製備成。在大多數情況下,此種機械敞開造成 比較大的連接胞室之孔隙。 適合於使用在本發明中之熱塑性樹脂包括可藉擠壓 程序發泡之所有型態熱塑性聚合物與摻合物。適於本發明 使用之熱塑性聚合物實例包括,但不限制於,聚苯乙烯與 聚烯烴樹脂類’包括聚乙烯樹脂,聚丙烯樹脂,以及乙烯 -笨乙烯共聚體(ESI)與聚烯烴樹脂類之摻合物,諸如聚 乙烯和ESI或聚丙烯與ESI和聚乙烯樹脂類之摻合物,聚乙 烯樹脂類之共聚物,以及聚乙烯樹脂類之掺合物為較佳者 。此種樹脂為低密度聚乙烯樹脂類,諸如具有約〇.4dg/ min之熔體指數以及〇.922g/cm3之密度者。 前述之乙烯-笨乙烯共聚體為一實質上無規之共聚體 ,以聚合形式包含i ) 一或一種以上之α-烯烴單體及乜 )一或一種以上乙烯基或亞乙烯基芳族單體類及/或一種 或一種以上空間位阻之脂族或環脂族乙烯基或亞乙烯基單 體類,以及可取捨之iii)其他可聚合之乙烯不飽和單體( 類)。 “共聚體”一詞在本文中係用來指一聚合物其中至 至少有兩種不同單體被聚合成為共聚體。 在由聚合i ) 一或一種以上之α -稀烴單體及ϋ) _ 或一種以上乙烯基或亞乙烯基芳族單體類及/或一種或— 種以上空間位阻之脂族或環脂族乙烯基或亞乙烯基單體類 ,以及可取捨之iii )其他可聚合之乙烯不飽和單體(類) 所生成之實質上無規共聚體t的“實質上無規”一詞在本 本紙張尺度適用中國國家橾準(CNS ) A4規格(210X29?公釐) -----7^-----裝---^--.™ 訂 (請先閱讀背面之注意事項再填寫本頁) 160518 A7 B7 經濟部中央標準局員工消費合作社印製 五、發明説明 文中一般是指該共聚想之單體分佈可由伯努利統計模型或 由一級或二級馬科維統計模型描繪,如同由J.C. Randall 在 POLYMER SEQUENCE DETERMINATION 之 Carbon-13 NMR 方法中所述,Academic Press New York,1977, ρρ·71-78。較佳地,由聚合一或一種以上a-烯煙單體與 一或一種以上乙烯基或亞乙烯基芳族單體類,以及可取捨 之其他可聚合乙烯不飽和單體(類)所生成之實質上無規 共聚體在三單元以上之乙烯基或亞乙烯基芳族單體嵌段中 不含有總量百分之十五以上的乙烯基或亞乙烯基芳族單體 。更佳者’共聚體不具有一高度全同立構規整度或間同立 構規整度之特徵。此意味在實質上無規共聚體之碳_13 NMR光譜中對應於代表内消旋二價基序列或外消旋二價 基序列之主鍵亞甲基和次甲基碳的峰區域應不超過主鏈亞 甲基和次甲基碳總峰區域之百分之七十五。其後使用之“ 實質上無規共聚體”一詞係指一由上述單體所製成之實質 上無規共聚體》 可用來製備實質上無規共聚體之適合^·烯烴單體包 括例如含有2至約·,較佳為2至12個,更佳為⑴個碳 原子之a _烯烴.尤其適合者為乙烯,兩烯,丁烯_丨,肛 甲基-1-戊稀,己稀-1或辛烯七丁缚.卜4甲基小戍稀, 己稀-1或㈣]之組合°最佳者為乙稀或乙稀與C3.8-“ 烴類之組合。這些a _類不含有_芳族部分。 其他可被應用來製備實無規共聚體之可取捨乙 烯基或亞乙稀基芳族單體包括例如由下式卜斤代表者 本紙張尺度it财g|國家標準(CNS ) A4規格( ——.--M J~II— —裝-- (請先閱讀背面之注意事項再填寫本頁) --訂 9 4Fig. 9 shows a cross section of a foaming ship according to the present invention, which is designated as I. Fig. 10 shows a cross section of a foaming body according to the present invention, which is indicated as U. Fig. 11 shows a cross section of a foam according to the present invention, and the cross section is designated as W. The present invention provides a thermoplastic polymer foam having sound-insulating properties that meet the needs of the application. The foam has mechanical strength, can be economically manufactured, and is hydrolytically stable. The foam of the present invention exhibits a combination of properties which have hitherto been difficult, if not impossible, to achieve. Therefore, the foam of the present invention exhibits one or more of the following properties: 1) an average cell size larger than about 2 mm; 2) a cell structure that is generally open; and 3) a relatively large pore connecting cells. In order for the foam to effectively sense sound, the foam should have a substantially open cell structure and a relatively low airflow resistance. According to the present invention, the foaming system with a generally open cell structure and relatively low airflow resistance is mechanically opened with an average cell size of about 2 mm or more. The paper size is applicable to China National Standard Car (CNS) A4 specifications (210 X 2? 7 mm) II--ί I----1 (Please read the notes on the back before filling out this page) 4 6051 8 A7 B7 Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs (5). In most cases, this mechanical opening results in relatively large pores connecting the cells. The thermoplastic resins suitable for use in the present invention include all that can be foamed by the extrusion process. Types of thermoplastic polymers and blends. Examples of thermoplastic polymers suitable for use in the present invention include, but are not limited to, polystyrene and polyolefin resins, including polyethylene resins, polypropylene resins, and ethylene-styrene Blends of interpolymers (ESI) and polyolefin resins, such as polyethylene and ESI or blends of polypropylene and ESI and polyethylene resins, copolymers of polyethylene resins, and polyethylene resins Blends of this type are preferred. Such resins are low density polyethylene resins, such as those having a melt index of about 0.4 dg / min and a density of 0.922 g / cm3. The body is a substantially random interpolymer comprising, in a polymerized form, i) one or more α-olefin monomers and ii) one or more vinyl or vinylidene aromatic monomers and / or one or one The above sterically hindered aliphatic or cycloaliphatic vinyl or vinylidene monomers, and optionally iii) other polymerizable ethylene unsaturated monomers (types). The term "interpolymer" is used herein to refer to a polymer in which at least two different monomers are polymerized into an interpolymer. In the polymerization i) one or more α-dilute hydrocarbon monomers and ii) _ or one or more vinyl or vinylidene aromatic monomers and / or one or more sterically hindered aliphatic or cyclic The term "substantially random" of the substantially random copolymer t produced by aliphatic vinyl or vinylidene monomers, and optionally iii) other polymerizable ethylenically unsaturated monomers (classes) is The size of this paper is applicable to China National Standard (CNS) A4 (210X29? Mm) ----- 7 ^ ----- pack --- ^-. ™ order (please read the precautions on the back first) (Fill in this page) 160518 A7 B7 Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs 5. The description of the invention generally refers to the distribution of the monomers of the copolymerization can be described by the Bernoulli statistical model or the primary or secondary Markovian statistical model , As described by JC Randall in the Carbon-13 NMR method of POLYMER SEQUENCE DETERMINATION, Academic Press New York, 1977, p. 71-78. Preferably, it is formed by polymerizing one or more a-ene smoke monomers and one or more vinyl or vinylidene aromatic monomers, and other polymerizable ethylenically unsaturated monomers (classes) that can be selected. The substantially random interpolymer does not contain more than 15% of the total vinyl or vinylidene aromatic monomers in the vinyl or vinylidene aromatic monomer blocks of three or more units. More preferred 'interpolymers do not have a feature of a high degree of isotacticity or syndiotacticity. This means that in the carbon-13 NMR spectrum of the substantially random interpolymer, the peak region corresponding to the methylene and methine carbons of the main bond representing the meso-divalent or meso-divalent sequence should not exceed 75% of the total peak area of the main chain methylene and methine carbon. The term "substantially random interpolymer" used thereafter refers to a substantially random interpolymer made of the above-mentioned monomers. Suitable olefin monomers that can be used to prepare substantially random interpolymers include, for example, olefin monomers such as Contains from 2 to about ·, preferably from 2 to 12, and more preferably an a-olefin of ⑴ carbon atoms. Particularly suitable are ethylene, diene, butene, anal methyl-1-pentane, hexane Dilute-1 or octene seven-butadiene. A combination of 4 methyl stilbene, dilute -1 or ㈣] ° The best is the combination of ethylene or ethylene and C3.8- "hydrocarbons. These a The _ class does not contain an aromatic moiety. Other desirable vinyl or ethylene aromatic monomers that can be used to make solid random interpolymers include, for example, the paper standard represented by the following formula: National Standard (CNS) A4 Specification (——.-- MJ ~ II— —Installation— (Please read the precautions on the back before filling this page) --Order 9 4

A7 B7 式A7 B7 style

Ar (严)n R1 — c = c (15) 其中R1係擇自於由氫和含有1至約4個碳原子之烷基 所組成之基團所組成之群組中者,較佳為氫或节基;每一 R係獨立地擇自於由氫和含有1至大約4個碳原子之烷基團 所組成之群組中者,較佳為氫或甲基;Ar為一苯基或一 由1至5個取代基所基代之苯基,該取代基擇自於由齒素, ci-4_烷基,以及Cw鹵代烷基所組成之群組中;且η具有一 自零至約4之值,較佳為零至2,最佳為零。特別適合的此 種單體包括笨乙烤和低院基_或其函代衍生物。較佳之單 體類包括苯乙烯,〇;_甲基笨乙烯,低烷基·( Ci_C4)或 苯乙烯之笨環取代衍生物,諸如舉例而言有鄰·,間-和對 甲基笨乙烯’ t-丁基笨乙烯,環鹵化笨乙烯類,諸如氣笨 乙婦,對-乙婦基甲苯或基混合物D 一較佳之芳族丁稀 單體為苯乙烯。 最佳之實質上無規共聚體為乙烯和苯乙烯之共聚體 以及乙烯、笨乙烯和至少一含有3至8個碳原子之α_烤烴 的共聚體。 實質上無規之共聚體通常含有自大約0.5至約65,較 佳為自大約1至約55,更佳為自約2至50莫耳百分比之至少 一乙烯基或亞乙烯基芳族單體或空間位阻脂族或環脂族乙 烯基或亞乙烯基單體,以及自大約35至約99 5,較佳為自 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) n. I ί ---n. I - in - ml - m : (請先鬩讀背面之注意事項再填寫本頁) 經濟部中央標準局員工消費合作社印製 10 - 4 6051 8 Α7 Β7 經濟部中央標準局員工消費合作社印製 五、發明説明(?) 大約45至約99 ’更佳為自大約50至約98莫耳百分比之至少 一具有2至約20碳原子之脂族α-稀烴。這些共聚體可依據 併於本文中供參考之W098/10014製備。 可取捨地’一成核劑可被加入可發泡摻合物。所使 用來製備本發明發泡體之成核劑量將依所需之胞室大小、 發泡溫度以及成核劑之組成變化。例如,當需要一大發泡 體尺寸時,應使用少量或不使用成核劑。有用的成核劑包 括碳酸鈣,硬脂酸鋇,硬脂酸鈣,滑石,黏土,二氧化鈦 ,矽,硬脂酸鋇,矽藻土,檸檬酸和碳酸氫鈉之混合物, 諸如此類者。當被使用時,所應用之成核劑量範圍係為以 重量計每一百份重量之聚合物樹脂摻合物〇〇1至約5份( pph)。 用來製造本發泡體之發泡劑包括所有業界習知型態 之發泡劑;物理和化學之發泡劑以及其混合物,包括無機 發泡劑,有機發泡劑和化學發泡劑。適當之無機發泡刺包 括二氧化碳,氮,氬,水,空氣及氦。有機發泡劑包括具 有1 -6破原子之脂族破氫化合物’具有1 ·3碳原子之脂族醇 類’以及具有1 -4個碳原子之完全或部分鹵化之脂族碳氫 化合物。赌族碳氫化合物包括甲院,乙院,丙院,丁院 ,異丁烷,η-戍烷,異烷,新戊烷,等等。脂族醇包括甲 醇,乙醇,η-丙醇,以及異戊醇。完全及部分鹵化之脂族 碳氫化合物包括含氣烴類,含氟烴類,以及含氣氟烴類。 使用在本發明中之含氣烴類包括氣代甲烷,二氣甲烷,氣 乙烷,1,1,1-三氣乙院,諸如此類。使用在本發明中之 本紙張尺度適财軸家料(CNS ) A4規格(210X 297公釐) u. -- -II - · SI- - i I m - - i X. (請先閱讀背面之注意事項再填寫本頁) 11 - 經濟部中央標準局員工消費合作社印製 6 0 51 8 a? B7五、發明説明(7 ) 含氟烴類包括氟代曱烷,二氟甲烷,氟代乙烷,1,1-二 氟乙烷(HFC-152a),1,1,1-三氟乙烷(HGC-143a),1 ,1 ’ 1,2-四氟乙烷(HFC-134a),1’1,2,2-四氟乙烷 (HFC-134),五I乙炫,全氟乙烧,2,2-二氟丙烧,1 ’ 1’卜三氟丙烧,1,1’ 1’3’3 -五氟丙烧,諸如此類 。使用於本發明中之部分氫化含氣氟烴類包括氣二氟(代 )甲烷(HCFC-22),卜 1-二氯-1-氟代乙烷(HCFC-141b ),1-氣-1-1-二氟代乙烷(HCFC-142b),1,1-二氣-2,2 ’ 2-三氟代乙烷(HCFC-123 ),1-氣-1,2,2,2-四氟代 乙院(HCFC-124 ) ’諸如此類。完全鹵化含氣氟烴類亦可 被使用但基於環境理由並非優選。使用在本發明中之化學 發泡劑包括偶氮二醞胺,偶氮二異丁腈,苯磺醯肼,4, 4_ 笨酚磺醯-氨基脲,P-甲笨磺醯氨基脲,N,N=-二甲基-N ,N =-二亞硝基對笨二醯胺,以及三肼三嗉,碳酸氫鈉 ’碳酸氫納與桴檬酸之混合物,諸如此類。所有這些發泡 劑之混合物亦被預想為本發明之範圍内。擠壓過程與製造 可模製珠類之分批法的較佳發泡劑為物理發泡劑,揮發性 有機發泡劑為較佳者’而低烴類(例如丙烷和丁烷)最佳 。交聯發泡體製程之較佳發泡劑為可分解發泡劑和氮。 被加入聚合物熔體材料以製成一形成發泡體之凝膠 的發泡劑量係依達成一定密度所需要者而變化。 本發明之發泡體可取捨地進一步包括一紅外吸收劑 (透射阻斷劑)諸如碳黑、石墨、二氧化鈦,諸如此類, 以提高隔熱能力。當被利用時,紅外線吸收劑可佔有約丨〇 本紙張尺舰财_家縣(⑽)A4規格(210~^^---- . I. - - I - —- - - - — II J1 ——- I (請先閲讀背面之注意事項再填寫本頁) -12 - 經濟部中央標準局員工消费合作社印裂 Α7 ______Β7 五、發明説明(π ) 與約25重量百分比之間且較佳為約2.0與約10.0重量百分 比之間’以發泡體中聚合物摻合物之重量為基礎。碳黑可 為任何習知型態者諸如爐法碳黑,乙炔黑,以及槽法碳黑 〇 最好本發明之發泡體呈現尺寸穩定性。在由前述發 泡體製造實質上閉合胞室構造之厚(例如> 4mm )片或板 條產品(厚於約12mm )時一穩定性控制劑可能為特別需 要者°相反地,當形成實質上敞開胞室發泡體時一額外之 穩定性控制劑可能並不需要或被需求。 尺寸穩定性係由量取老化期間發泡體體積的發泡體 起始體積百分比,在發泡體發泡後的3〇秒内測量。使用此 一定義’一在一個月内恢復80%之發泡體係為可容許者, 然而恢復85%或更多者係為較佳,且一恢復9〇%或更多之 發泡體尤其為佳。體積係藉由一適當方法諸如水之體積置 換測定8 較佳之穩定性控制劑包括醯胺類和C|G.24脂肪酸之酯 類。此種控制劑係教示於併於本文中供參考之美國專利第 36M230及4214054號中。最佳之控制劑包括十 八晚酿十八 院醯胺’甘油一硬脂酸’甘油,以及山梨糖 醇一硬脂酸。典型地’此種穩定性控制劑係以一從每一百 份聚合物大約0_1至大約10份範圍之量被使用。 各種不同的添加劑亦可被加入發泡體中,諸如無機 填料’色素’抗氧化劑’酸清除劑,紫外線吸收劑,阻燃 劑,操作助劑,掩壓助劑,諸如此類。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -----7^----—^.-- (請先閲請背面之注意事項再填、寫本頁) -* 13 4605 1 8 A7 B7 經濟部中央標準局員工消費合作社印製 五、發明説明(// ) 本發明之聚合物發泡體可藉由習此技藝者熟知之技 術和程序包括利用—可分解發泡劑和交聯劑之擠壓程序以 及分批程序製備,以擠壓程序為佳。 在一擠壓程序中,胞室大小係受到數項參數影響, 包括發泡劑之類型與含量,聚合物類型,模具口型之幾何 形狀,模具之剪切速率’成核劑之含量’胞室增大劑之使 用’以及發泡溫度。為了使胞室尺寸大,胞室成核劑通常 不加入。代之可添加一胞室增大劑。在其餘的參數中,發 泡劑之類型與含量對胞室尺寸有最大的影響。通常具有一 相當高的溶解度與一小分子尺寸之發泡劑在一相當低之含 量下可提供一大胞室尺寸。此種發泡劑之例子包括丙炫, η-丁烷,異丁烷,η-戊烷,氯代甲烷,二氣甲烷,氣乙烷 ,甲醇,乙醇,二甲醚,水,以及含有這些發泡劑之一者 或一者以上的混合發泡劑。藉由高壓自由基方法所製備之 支化烯聚合物樹脂當由這些發泡劑發泡時易於提供大胞室 。胞室尺寸增大添加劑一般而言為使用在塑化聚合物樹脂 中之化合物。胞室尺寸增大劑之例子包括如同併入本文中 供參考之美國專利第4229396號中所記載之具有一相當低 炼點之臘狀材料*以及如同併入本文中供參考之美國專利 第5489407號中所揭露之非臘狀低分子量化合物。 本發明之聚合物發泡體可為交聯或非交聯者。製造 聚合物發泡體構造並加工此等發泡體之方法係教示於併於 本文中供參考 ’ Hanser Publishers,Munich, Vienna, New York, Barcelona ( 1991 )出版,由 D.KIempner 與K.C.Frisch 本紙張尺度適用中國國家#準(CNS ) A4規格(2]0X297公釐) (請先閱讀背面之注意事項再填寫本頁) J-----^------—,π------^---1__________.__„__Ar (strict) n R1 — c = c (15) where R1 is selected from the group consisting of hydrogen and an alkyl group containing 1 to about 4 carbon atoms, preferably hydrogen Or benzyl; each R is independently selected from the group consisting of hydrogen and an alkyl group containing 1 to about 4 carbon atoms, preferably hydrogen or methyl; Ar is a phenyl or A phenyl group substituted by 1 to 5 substituents selected from the group consisting of halide, ci-4_alkyl, and Cw haloalkyl; and η has a number from 0 to about 4 The value is preferably zero to two, and most preferably zero. Particularly suitable monomers of this type include benzyl and low-density bases or their functional derivatives. Preferred monomers include styrene, 0; -methylbenzylethylene, lower alkyl (Ci_C4) or benzene-substituted substituents of styrene, such as, for example, o-, m-, and p-methylbenzyl 't-Butylbenzyl, cyclic halogenated vinyls, such as ethylbenzene, p-ethynyltoluene, or base mixture D. A preferred aromatic butadiene monomer is styrene. The most preferred substantially random interpolymers are interpolymers of ethylene and styrene as well as interpolymers of ethylene, stupid ethylene and at least one α-grilled hydrocarbon containing 3 to 8 carbon atoms. Substantially random interpolymers typically contain from at least one vinyl or vinylidene aromatic monomer or from about 0.5 to about 65, preferably from about 1 to about 55, and more preferably from about 2 to 50 mole percent Sterically hindered aliphatic or cycloaliphatic vinyl or vinylidene monomers, and from about 35 to about 99 5, preferably from this paper size. Applicable to China National Standard (CNS) A4 specification (210X 297 mm) n I ί --- n. I-in-ml-m: (Please read the notes on the back before filling out this page) Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs 10-4 6051 8 Α7 Β7 Central of the Ministry of Economic Affairs Printed by the Bureau of Standards Consumer Cooperatives 5. Description of the invention (?) About 45 to about 99 ', more preferably from about 50 to about 98 mole percent, at least one aliphatic alpha-dilute hydrocarbon having 2 to about 20 carbon atoms. These interpolymers can be prepared according to W098 / 10014, which is incorporated herein by reference. Desirably, a nucleating agent may be added to the foamable blend. The amount of nucleating agent used to prepare the foam of the present invention will vary depending on the required cell size, foaming temperature, and composition of the nucleating agent. For example, when a large foam size is required, a small or no nucleating agent should be used. Useful nucleating agents include calcium carbonate, barium stearate, calcium stearate, talc, clay, titanium dioxide, silicon, barium stearate, diatomaceous earth, a mixture of citric acid and sodium bicarbonate, and the like. When used, the nucleation dose range is from 0.01 to about 5 parts (pph) per hundred parts by weight of the polymer resin blend. The foaming agents used to make the foam include all types of foaming agents known in the industry; physical and chemical foaming agents and mixtures thereof, including inorganic foaming agents, organic foaming agents, and chemical foaming agents. Suitable inorganic foaming thorns include carbon dioxide, nitrogen, argon, water, air and helium. Organic blowing agents include aliphatic hydrogen decomposers having 1 to 6 atomic break-ups' aliphatic alcohols having 1.3 carbon atoms and fully or partially halogenated aliphatic hydrocarbons having 1 to 4 carbon atoms. Gambling hydrocarbons include House A, House B, House C, House D, Isobutane, η-Pane, Isoane, Neopentane, and so on. Aliphatic alcohols include methanol, ethanol,? -Propanol, and isoamyl alcohol. Fully and partially halogenated aliphatic hydrocarbons include gaseous hydrocarbons, fluorocarbons, and gaseous fluorocarbons. Gas-containing hydrocarbons used in the present invention include gas-substituted methane, digas-methane, gas-ethane, 1,1,1-three-gas, and the like. The paper size used in the present invention is CNS A4 (210X 297mm) u.--II-· SI--i I m--i X. (Please read the back Note: Please fill in this page again) 11-Printed by the Consumer Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs 6 0 51 8 a? B7 V. Description of the invention (7) Fluorocarbons include fluoromethane, difluoromethane, fluoroethyl Alkane, 1,1-difluoroethane (HFC-152a), 1,1,1-trifluoroethane (HGC-143a), 1,1 '1,2-tetrafluoroethane (HFC-134a), 1'1,2,2-tetrafluoroethane (HFC-134), pentafluoroethane, perfluoroethane, 2,2-difluoropropane, 1 '1', trifluoropropane, 1,1 '1'3'3-pentafluoropropane, and the like. The partially hydrogenated gas-containing fluorocarbons used in the present invention include gas difluoro (methane) methane (HCFC-22), 1-dichloro-1-fluoroethane (HCFC-141b), 1-gas-1 -1-difluoroethane (HCFC-142b), 1,1-digas-2,2 '2-trifluoroethane (HCFC-123), 1-gas-1, 2, 2, 2, 2- Tetrafluoromethane A (HCFC-124) 'and the like. Fully halogenated fluorocarbons can also be used but are not preferred for environmental reasons. The chemical foaming agents used in the present invention include azodiamine, azobisisobutyronitrile, sulfenylhydrazine, 4, 4-benzylsulfonium-carbazide, P-methylbenzylsulfonamide, N , N = -dimethyl-N, N = -dinitroso-p-dibenzidine, and a mixture of trihydrazine, sodium bicarbonate, sodium bicarbonate and citric acid, and the like. Mixtures of all these blowing agents are also contemplated as being within the scope of this invention. Physical foaming agents are the preferred blowing agents for extrusion processes and batch processes for making moldable beads. Volatile organic foaming agents are preferred. Low hydrocarbons (such as propane and butane) are the best. . The preferred blowing agents for the crosslinked foaming system are decomposable blowing agents and nitrogen. The amount of foam to be added to the polymer melt material to form a foam-forming gel varies depending on what is needed to achieve a certain density. The foam of the present invention may optionally further include an infrared absorber (transmission blocker) such as carbon black, graphite, titanium dioxide, and the like, so as to improve the heat insulation ability. When used, the infrared absorber can occupy about 丨 0 paper ruler _ home county (⑽) A4 specifications (210 ~ ^^ ----. I.--I-------II J1 ——- I (Please read the precautions on the back before filling this page) -12-Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs Α7 ______ Β7 V. Description of the invention (π) and about 25% by weight and preferably Between about 2.0 and about 10.0 weight percent is based on the weight of the polymer blend in the foam. Carbon black can be any conventional type such as furnace black, acetylene black, and channel black. It is good that the foam of the present invention exhibits dimensional stability. When a thick (for example > 4mm) sheet or slat product (thicker than about 12mm) of a substantially closed cell structure is manufactured from the foregoing foam, a stability control agent May be particularly needed. Conversely, an additional stability control agent may not be needed or required when forming a substantially open cell foam. Dimensional stability is measured by measuring the volume of foam that develops during aging. Foam starting volume percentage, measured within 30 seconds after foaming Use this definition 'one that recovers 80% of the foaming system within a month is tolerable, but recovering 85% or more is better, and one that recovers 90% or more of the foam is especially Volume is determined by a suitable method such as volume displacement of water. 8 Preferred stability control agents include amidoamines and C | G.24 fatty acid esters. Such control agents are taught and provided herein. Refer to US Patent Nos. 36M230 and 4214054. The best control agents include eighteen nights stearylamine 'glycerol-stearate' glycerol, and sorbitol-stearic acid. Typically 'this kind of stability Sex control agents are used in an amount ranging from about 0 to about 10 parts per hundred parts of polymer. Various additives can also be added to the foam, such as inorganic fillers 'pigment', antioxidant, and acid scavenger. , UV absorber, flame retardant, operation aid, masking aid, etc. This paper size applies Chinese National Standard (CNS) A4 specification (210X297 mm) ----- 7 ^ ------ ^ .-- (Please read the notes on the back before filling and writing this page)-* 13 4605 1 8 A7 B7 Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs 5. Description of the invention (//) The polymer foam of the present invention can be used by techniques and procedures familiar to those skilled in the art, including the use of decomposable foam The extrusion process and batch process of the agent and cross-linking agent are preferably prepared by the extrusion process. In an extrusion process, the cell size is affected by several parameters, including the type and content of the foaming agent, and the polymer Type, mold mouth geometry, mold shear rate, content of nucleating agent, use of cell enlarger, and foaming temperature. In order to make cell size large, cell nucleating agent is usually not added. A cell enlargement agent may be added instead. Among the remaining parameters, the type and content of the foaming agent has the greatest effect on cell size. Foaming agents which generally have a relatively high solubility and a small molecular size can provide a large cell size at a relatively low content. Examples of such blowing agents include propane, η-butane, isobutane, η-pentane, methyl chloride, digasmethane, gaseous ethane, methanol, ethanol, dimethyl ether, water, and those containing these One or more foaming agents are mixed foaming agents. The branched olefin polymer resin prepared by the high-pressure radical method easily provides a large cell when foamed by these blowing agents. Cell size increasing additives are generally compounds used in plasticized polymer resins. Examples of cell size increasing agents include wax-like materials with a relatively low refining point as described in U.S. Patent No. 4,229,396 incorporated herein by reference; and U.S. Patent No. 5,489,407 as incorporated herein by reference Non-wax low molecular weight compounds disclosed in No. The polymer foam of the present invention may be crosslinked or non-crosslinked. Methods of making polymer foam structures and processing these foams are taught and incorporated herein by reference 'Hanser Publishers, Munich, Vienna, New York, Barcelona (1991), published by D.KIempner and KCFrisch Paper size applies to China National Standard #CNS (A4) (2) 0X297 mm (Please read the notes on the back before filling this page) J ----- ^ --------, π-- ---- ^ --- 1 __________.__ „__

—^ϋ II 14 A7 460518 五、發明説明(β ) 〜 編輯之C.P.Park,Polyolefin Foam, Chapter 9, Handbook of Polymer Foams and Technology 中教示 〇 本發明之非交聯發泡體可由一習知擠壓發泡鞋序製 造。發泡體構造一般係藉由加熱一熱塑性聚合物樹脂(即 聚合物材料)以形成一塑化或溶體合物材料,其中加入— 發泡劑以形成一可發泡凝膠,且將凝膠擠經一模具而形成 發泡體產品。在與發泡劑混合之前,聚合物材料被加熱至 一玻璃化轉變溫度或熔點以上之溫度。發泡劑可藉由任何 習知裝置諸如藉由一擠壓機,混合器,摻合機等被加入或 混合至熔體聚合物材料中,發泡劑係與溶體聚合物在一昇 高而足以避免熔體聚合物材料之實質上發泡的壓力下混合 且將發泡劑均勻地散佈其内《可取捨地,一成核劑可掺合 於聚合物熔體十或在塑化或熔化前與聚合物材料乾摻合。 可發泡凝膠典型地被冷卻至一較低溫度以使發泡體構造之 物理特性最佳化。凝膠接著被擠壓或輸送經過一具有所欲 形狀之模具至一減壓或具較低壓力區域而形成發泡體構造 。較低壓力區域係在一低於可發泡凝膝在擠經模具前所被 維持之壓力之下該較低壓力可為超計大氣壓或低於一大 氣壓(真空),但最好是在一大氣壓水平。 本發明之非交聯發泡體係藉由將熱塑性聚合物樹脂 (即聚合物材料)擠經一多口型模具而以一結合多股型式 被形成。該等口型係配置成使得熔融擠壓物之相鄰流之間 的接觸在發泡程序期間發生且接觸表面以足夠之黏合力彼 此黏合而生成一單元之發泡體構造。離開模具之熔融擠壓 本紙張尺度朝巾關家辦(CNS ) Α4聽(210 X 297公釐) (請先閔讀背面之注意事項再填寫本頁} 丨裝. 經濟部中央標準局員工消費合作杜印策 15 4 6〇518 A7 B7 娌济部中央標準局負工消費合作杜印製 五、發明説明(G ) 物流呈多股或型面之型式,希求為發泡體,組合,並彼此 黏合而形成一單元構造,依照想望,結合之個別股或型面 應維持黏合成一單元構造以避免股在製備、成形、以及利 用發泡體時所遇之應力而層離。製造結合股型式之發泡體 構造的裝置與方法係教示於併 入本文以為參考之美國專利 第 3573152及4324720號中。 本發泡體構造亦可被形成為適於模塑成物件之非交 聯發泡體珠粒。發泡體珠粒可由—擠壓程序或一分批程序 製備。在擠壓程序中,由一附於一習知發泡體擠壓裝置之 多孔模具中出來的發泡體細條係被粒化形成發泡體珠粒。 在一分批程序中,個別的樹脂粒諸如粒化之樹脂丸係懸浮 在一其所實質上不溶解之液體介質如水令;藉由將發泡劑 在一壓熱器或其他壓力容器中於提高壓力和溫度下導入液 體介質而被發泡劑浸透;且迅速地排出至大氣壓或一減壓 區域中以發泡形成發泡體珠粒。此一程序係教示於併入本 文中供參考之美國專利第4379859和4464484號中。 本發明之交聯發泡體係藉由應用一可分解之發泡劑 的交聯發泡體程序或藉由習知之擠壓程序製備。 當利用該使用一可分解發泡劑之交聯發泡體程序時 ’本發明之交聯發泡體可藉摻合並加熱塑性聚合物樹脂( 即’聚合物材料)與一可分解化學發泡劑而形成一可發泡 塑化或熔體聚合物料,將可發泡熔體聚合物材料擠經一模 具1在熔體聚合物材料内引起交聯,並使熔體聚合物材料 曝露至一昇高溫度以釋出發泡劑而形成發泡體構造。聚合 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) ~I訂 (請先閱讀背面之注意事項再填寫本頁) 16 460518 A7 -----_B7 五、發明説明(/4 ) 物材料和化學發泡劑可被混合且藉由任何習知技藝中之裝 置諸如藉一擠壓機,混合器,摻合機等熔體摻合。化學發 泡劑最好與聚合物材料在聚合物材料加熱成一熔體形式前 乾摻合’但亦可於聚合物材料呈熔體相時被加入^交聯可 由加入一交聯劑或藉輻射引起。引起交聯與曝露於一昇高 溫度以造成發泡或膨脹可同時或相繼發生。如果一交聯劑 被使用’其係以與化學發泡劑相同.之方式被加入Q此外, 如果一交聯劑被使用,可發泡熔體聚合物材料被加熱或曝 露至一最好低於15〇°c之溫度以避免交聯劑或發泡劑分解 且避免過早交聯。如果輻射聯被應用,可發泡熔體聚合物 材料被加熱至一最好低於160它之溫度以避免發泡劑分解 °可發泡炼體聚合物被擠壓或輸送經過一具有所欲形狀之 模具而形成發泡體構造。可發泡構造接著在一升高或高溫 下(典型為150°C -250。(:)諸如於一烘箱内發泡以形成一 發泡體構造。當輻射交聯劑被利用時,可發泡構造被照射 以交聯聚合物材料’其即在上述之升高溫度下發泡。該構 造可依據上述利用交聯劑或輻射任一者之程序有利地製成 片或薄板條形式。 經濟部中夬標隼局員工消費合作社印製 -- i — I ,4i ---I ---1__!_ 訂 (請先閲讀背面之注意事項再填寫本頁) 除了在應用一可分解發泡劑之交聯發泡體程序中使 用一交聯劑或輻射之外’交聯亦可藉由如c.p.park, Chapter9中所記述之矽烷交聯而達成。 本發明之交聯發泡體亦可利用一如GB 2145961A號中 所敘述之長脊模具被製成一連續之板條構造+,該專利併 入本文中供參考。於該程序中,聚合物,可分解發泡劑以 本紙浪尺度適用中國國家標準(CNS ) A4規格(210χ297公釐) 17 A7 460518 _____B7 五、發明説明(if ) ~ 及交聯劑係在一擠壓機中被混合;混合物被加熱以使聚合 物交聯且發泡劑在一阿脊模具中分解;且發泡體構造被成 形並離開模具被處理,發泡體構造與模具接觸係由一適當 之潤滑材料潤滑。 本發明之交聯發泡體亦可被形成適合模製成物件之 父聯發泡體珠粒。欲製造發泡體珠粒,分離之樹腊粒子諸 如粒化樹脂丸係懸浮在一其所實質上不溶於之液體介質諸 如水中;以一交聯劑和一發泡劑在一升高壓力與溫度下於 一壓熱器或其他壓力容器中浸透;並迅速地排至大氣壓或 一減壓區域中以使發泡體珠粒膨脹。在此程序之另一種型 式中’聚合物珠粒以發泡劑浸透’被冷卻,從容器中排出 並接著藉由加熱或以蒸氣發泡。在上述程序之一種衍生型 式中’笨乙稀單體可與交聯劑一同被浸透至懸浮之丸中以 开> 成與聚合物材料之一種接枝共聚體。發泡劑可在懸浮時 、或者在一不含水狀態下被浸透至樹脂丸内。可發泡之珠 粒接著由以蒸氣加熱被發泡且藉由一習知之可發泡聚苯乙 烯發泡體珠粒成型方法成型。 發泡體珠粒然後可藉由任何習知手段,諸如將發泡 體珠粒裝料至塑模中,壓緊縮模以壓·縮珠粒,並加熱珠粒 、諸如以蒸氣加熱以造成珠粒聚結且熔接而形成物件。可 取捨地,珠粒可以空氣或其他發泡劑在裝料至塑模前先預 熱。上述程序及成型方法的極佳教示可見於C p park pp_227-233 ’ 美國專利第 3886100, 3959189,4168353 及4429059號中,皆併於本文中供參考D發泡體珠料亦可 &張尺度it财咖家辟(CNS )鐵格(210X297公釐) ---- -18 * (請先聞讀背面之注意事項再填寫本頁) —裝. 經濟部中央標準局員工消費合作社印製 460518 Λ7 B7 五、發明説明(/公) ~ 藉由在-適當混合裝置或擠壓機藉製備—聚合物'交聯劑 i m ^it m ϊχ— ^^^1 ^^^1 .1 ^^^1 ^^^1 ^^^1 ^^^1 - (諳先聞讀背面之注意事項再填寫本頁) ,以及可分解混合物之混合物而製请,且將混合物形成丸 ,並加熱該丸以交聯並發泡。 另-種製造適合於成型為物件交聯發泡體珠粒之方 法為熔化聚合物材料且將其與—物理發泡劑在一習知發泡 體擠壓裝置中混合以形成-實質上連續之發泡體細條。此 發泡體細條被粒化或製丸而形成發.泡體珠粒。此發泡體珠 粒可接著被聚結並成型而形成上述各種不同物件以供另一 發泡體珠粒程序之用。此程序之其他教示可見於美國專利 第3616365號及C_P. Park.仏/?〜,pp,224-228,皆併於本文 中供參考。 此外’矽烷交聯技術可被應用在擠壓程序中,此一 程序之教示可見於C.P. Park. SwprflXapter 9以及美國專 利第4714716號中’二者皆併入本文中供參考。當石夕烧交 聯程序以習知之擠壓製程一起被利用時,一聚合物以一乙 烯基官能矽烷或一疊氮基官能矽烷接枝且被擠壓而形成發 泡體。擠壓之發泡體接著被曝露於溫暖潮濕之空氣以使交 聯逐漸產生。 經濟部中失標隼局員工消費合作社印製 本發明之交聯發泡體係藉由混合聚合物材料,一交 聯劑,以及一發泡劑以一泡沫膠塊原料形式製成以形成一 厚塊,在一塑模中加熱混合物使交聯劑能夠交聯聚合物材 料且發泡劑能分解,並且藉由在塑模中釋放壓力而使發泡 體膨脹。可取捨地,在釋放壓力時所形成之泡洙膠塊原料 可再加熱以造成進一步膨脹。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) 19 經濟部中央榡準局員工消費合作杜印製 6 Ο 5 1 8 Α7 — _____Β7__ 五、發明説明(/,) 交聯聚合物薄片係由以一高能量射線照射一聚合物 薄片或由加熱一含有一化學交聯劑之聚合物薄片而被製成 。交聯聚合物薄月被切割成所需要的形狀且在高壓下以及 一高於聚合物軟化點之溫度下以氮滲透。釋放壓力造成氣 泡之成核以及薄片中之一些膨脹。此薄片在一低壓容器中 在高於軟化點之壓力下再加熱,且壓力被釋放而使得發泡 體膨脹。 由以上方法所製備成之發泡體呈現由大約10 kg/m3 至大約300kg/m3之密度,具有約15 kg/m3至約100 kg/ m3較佳’且具有約15 kg/m3至約60 kg/m3密度之發泡體 特別合意。此外,由以上方法所製備之發泡體呈現一約2mm 至15mm之平均胞室尺寸,合意之胞室尺寸為2mm至i〇mm ’約3mm至約10mm更佳,且自大約4mm至約8mm則特別 合意。此外’由以上方法所製備之發泡體可為敞開胞室或 閉合胞室者。 依據上述方法所製備之發泡體在聲音管理上毋需額 外處理步驟即可利用。例如,由上述方法所製備成具有一 大於約4 m m之平均胞室尺寸之發泡體不考慮其他發泡體所 具有之性質可呈現一適合使用作一聲音吸收材料的充分低 氣流阻力,且不需額外處理步驟。典型地,對於聲音管理 最後使用者而言,低於約800000 Ray丨s/m (即800000 Pa s /m2 )為所需要者,依發泡體之最後用途而定,低於 400000 Rayls/m(即 400000 pa s/m2 ),低於 looooo Ray】s /m (即 100000 pa s/m2 ),以及低於50000 Rayls/m ( 本紙張尺度適用中國國家棲準(CNS ) A4規格(2i〇X297公釐〉 n 1 - - - - - - 11. I - - - - --- -- >^D (請先聞讀背面之注意事項再填寫本頁) 20 4 60518 A7 B7 五、發明説明(Μ ) 即50000 Pa s/m2 )逐次更加理想。 但是,如果以上述方法製備之基礎發泡體未呈現充 分之聲音管理性質’添加或加強性質諸如I)實質上敞開胞 室構造或2)相當大的連接胞室孔隙’可藉由以機械裝置 敞開基礎發泡體中之閉合胞室而授予至基礎發泡體。 經濟部中央標準局員工消費合作社印製 ,I --- —^1 二 ^^1 ^^1 _ - - m» (請先閱讀背面之注意事項再填寫本頁) 如前所述,為了使發泡體有效感,發泡體應具有一 實質上敞開胞室之構造以及一相當低的氣流阻力。依據本 發明,具有實質上敞開胞室構造與相當低之氣流阻力之發 泡體係藉由機械地敞開一具有大於約2mm之平均胞室尺寸 的發泡體而製備。在大多數情況中,此種機械敞開造成相 當大的連接胞室孔隙。例如,發泡體内之閉合胞室可藉由 在一多孔狀熱塑性聚合物發泡體中應用一裝置敞開閉合胞 室而被敞開至少某些部分或基礎熱塑性聚合物發泡體之至 少一表面’此一應用足以造成在基礎聚合物發泡體内之閉 合胞室某些部分被敞開。閉合胞室被機械裝置敞開之部分 自然乃依敞開閉合胞室之裝置所應用的範圍而定。例如, 若一較小百分比之閉合胞室被敞開,裝置之應用將只施行 於基礎發泡體之一部分及/或僅部分伸展通過基礎發泡體 之厚度。但是,如果一較大百分比之閉合胞室被敞開,敞 開用裝置之應用將被施行於更多的基礎發泡體表面及/或 更深地延伸入基礎發泡體之厚度。 敞開閉合胞室之裝置的應用方向並不重要且可垂直 或與擠壓方向相同地實施,且可以任何相對基礎發泡體表 面之角度實施° 本紙張尺度適用中國國家榡準(CNS ) A4規格(210 X 297公釐) 21 Η π 5 1 8 at __Β7 五、發明説明) 敞開閉合胞室之手段可為任何足以敞開閉合胞室之 手段,但典型者包括穿孔’切斷,壓縮,或其組合。典型 地,穿孔包括以一或一個以上尖頭、銳利之物體穿刺基礎 發泡體。適當的尖頭、銳利物體包括針、刺針、銷、釘等 類。此外,穿孔包括射L、雷射切割、高壓流體切割、氣 搶,或彈丸。第1圖描繪本發明由許多閉合胞室2組成之一 基礎發泡體丨之橫截面,發泡體丨係以許多尖頭、銳利之物 體3穿孔。 此外,基礎發泡體可藉由在膨脹期間拉伸發泡體細 條被製備成具有長形胞室。此種拉伸產生長形胞室而不改 變、或常常增加在水平方向上之胞室尺寸。因此,拉伸造 成在垂直於垂直方向的方向上的一增加水平胞室尺寸(Eh 平均)且便於穿孔。第2圖描緣本發明由許多閉合胞室所 組成之基礎發泡體1之橫截面’該閉合胞室已在被許多央 頭、銳利物體3穿孔之擠壓方向4上被伸長。第3圖福繪本 發明由許多閉合胞室所組成之基礎發泡體丨之橫截面該 閉合胞室已在被許多尖頭、銳利物件3以一傾斜角度穿孔 之擠壓方向4上被伸長。 經濟部中央標隼局舅工消費合作社印製 . -~1 I J— I - I . I I: I (請先閱讀背面之注^K項再填寫本頁) 基礎發泡體之穿孔可以任何式樣被穿孔,包括正方 形式樣及二角形式樣。此外,最好穿孔間之距離相同於發 泡體内之胞室大小俾貫穿大多數之胞室。因此,當希望大 部分的胞室被穿孔時’最好穿孔是由一造成以不大於基礎 發泡體内胞室平直徑兩倍’較佳為不大於15倍,更佳為 等於基礎發泡體内胞室平均直徑,且最佳者為小於基礎發 本紙張尺度適用中國國家標準(CNS ) Λ4規格(210X297公董) 22 經-.部中夬標進局員工消費合作社印製 A 7 B7 五、發明説明(^ ) 泡體内胞室之平均直徑之距離彼此分隔之穿孔的方式實施 。雖然一特別直徑之銳利、尖頭、用來貫穿基礎發泡體之 物體的選擇依許多因素而定,包括平均胞室尺寸,所欲之 穿孔間距等,可用於製備本發明某些發泡體之尖頭、銳利 物體典型地具有約1 mm至約4mm之直徑。 切割可藉由任何足以切穿至少一部分發泡體之裝置被 實施’且包括刀、鋸等類。藉由切割來敞開基礎發泡體之 胞室必然只需要敞開在切割表面之胞室,留下在發泡體内 部之胞室未改變。因此,切割未減少整個發泡體厚度之氣 流阻力。但是’藉由切割敞開表面胞室對於某些聲音管理 應用為足夠,尤其是如果胞室尺寸足夠大且/或留下未切 割之發泡體足夠薄。雖然未受到任何特別的理論拘限,本 案發明人相信為了有效吸枚聲,不需要整個發泡體厚度皆 為低氣流阻力。此係因聲音為空氣之壓力波,其係藉由空 氣分子以一振動方式運動(即,空氣分子以一固定平均位 置前後運動*碰撞在空氣相鄰層之分子)而傳導。空氣本 身不向發泡體厚度移動一大距離。因此,在聲音傳遞過一 發泡體基質期間無真正的空間流動。但是,聲音係藉由空 氣向前後運動時所形成之熱消散,造成胞室壁之一摩擦。 由於分子以一大抵上垂直於其其運動方向撞擊一薄膜上之 分子’屬一壓力波之聲波通過一阻擋其通道之軟膜造成薄 膜振動並依次造成另一側之空氣振動。因此,可撓薄膜之 少數層,諸如本發明表面胞室已被切割之發泡體未改變内 部核心不會過度傷害發泡體之聲音吸收能力。 本紙張尺度適用中國國家橾率(CNS ) A4規格(210X 297公釐) ^^1 m. I HI m ^^1 ......... I— HI «II 1^1 (請先閱讀背面之注意事項再填寫本頁} 23 A7 60510 ____B7 五、發明説明(2/ ) 作為敞開胞室之一手段的壓縮可藉由任何足以施加外 力至發泡體之一或一個以上表面的裝置實施,且因此造成 基礎發泡體内之胞室破裂及敞開。因造成通過胞室壁之高 壓力差,故在穿孔期間或穿孔之後的壓縮在裂開鄰接由穿 孔所造成之槽道的胞室壁上尤其有效。此外,不像針鑽孔 ’壓力可產生面對所有方向的裂開胞室壁,俾造成聲音吸 收所需要之曲折路徑。 基礎發泡體之閉合胞室的機械敞開藉由在胞室壁和支 柱中大尺寸孔隙而降低基礎發泡體的氣流阻力〇無論如何 ’不管執行的特定裝置為何,此種在基礎熱塑性聚合物發 泡體内之閉合胞室的敞開可提高聲音吸收,隔聲,流體吸 收’以及發泡體之過濾性質。 當然,被機械敞開之胞室百分比將有賴於許多因素, 包括胞室尺寸,胞室形狀,敞開之手段(即,穿孔,切割 ’壓縮),敞開手段施用至基礎發泡體的應用範圍等。為 了使氣流阻力減少得最多,最好在基礎發泡體内之閉合胞 室有大於50%係被上述之機械裝置敞開,更佳者為大於7〇 % ’且最佳為大於90%。為了使機械敞開之胞室的百分比 最大化’最好以壓縮與穿孔之組合被用來敞開胞室。第4 圖描繪本發明由許多在已經被首次壓縮之擠壓方向4上被 伸長之胞室所組成之基礎發泡體1的橫載面,且接著當發 泡體被壓縮時,以許多尖頭、銳利體3穿孔》 除了前面所討論的在擠壓前加入一阻燃劑至聚合材料 的選擇之外,本發明之發泡體亦可在其被擠壓後、最好在 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐〉 - -I -—-I - : - - — ^^1 ^^1 - - - I : (請先閱讀背面之注意事項再填寫本頁) 經濟部中夬標準局負工消费合作社印製 24 46〇518 Α7 Β7 經濟部智慧財產局員工消費合作社印製 五、發明説明(之z ) 其已接受任何其他處理步驟’諸如藉由拉伸而伸長以及閉 合胞室之機械敞開之後以一阻燃劑浸透。 當使用在隔音時’本發明之發泡體可在一多層隔音 板中當作核心層被使用,該多層隔音板由一覆面層,被附 貼於其上之發泡體核心層’以及核心層藉由長條、片、斑 點或其他幾何形狀之突出部(下文中一般稱作接觸點)以 分離之接觸點固定之構造所構成’在核心層與該構造之間 留有間隙’且在長間隔及/或薄覆面層的情況下,,_丨齡 議I以使核心層與該構造保持某種距離。核心層以分離之接 觸點被固定的該一構造可為一壁或一天花板或任何其他適 當之結構元件。或者,該構造可為一第二覆面層。所生成 之夾層板可被使用作一隔板元件或隔牆。此板可使用在建 築和其他工業上以改進建築物及/或機械裝置之隔音性質 β此種板之實例係記載於1995,5,26公告之W0 95/14136 中,其内容併入本文供參考。 當在一多層板中被使用作一核心層時,本發明之發 泡體可以被成型成一任何型式之輪廓。例如,本發明之發 泡體可被製成直線形狀之縱剖面。第9圖描繪本發明一縱 剖面製成由呈直線形型式,標示為I之發泡體核心5所構成 之發泡體。但是’本發明之發泡體亦可製成呈現一低動態 剛性之縱剖面。例如’本發明之發泡體可被製成由一發泡 體核心5所組成的縱剖面’同一或另一發泡體6之窄條已被 貼附在此發泡體核心5之同一端或兩端。第〗〇圖之縱剖面 標示為U。此外,本發明之發泡體可被製作成由一發泡體 (請先閱讀背面之注意事項再填寫本頁) * 〆 4· 25 4 6051 8 A7 B7 五、發明説明) 核心5所組成的縱剖面,同一或另一發泡體6之窄條已被間 隔地貼附在此發泡體核心5之相反兩邊且同一或另一發泡 體6之窄條已被貼附至此發泡體核心5之兩邊且在發泡體核 心5之兩端彼此相對。第11圖標示為w。當本發明之發泡 體製作成如此之縱刻面且置於面板之間,這些設計將對面 板之壓縮應變轉化成一對發泡體掠心之彎曲應變。假变支 持條之間有一足夠之距離’該構造提供所需要之非常低動 態剛性。在縱剖面W之例子中,發泡體核心5同一側之窄 條6中點間之距離至少為250mm ’且較佳者係在約3〇〇mrn 與約600mm之間。在縱剖面U之例子中,窄條中點之間的 距離係至少為350mm ’且較佳者係在約450mm與600mm之 間。 本發明之發泡體的以下實例不被解為限制用。除非 另有所指,所有的百分比' 份數及比例皆以重量計。 實例1 出程序製備此發泡體的一方法。如表1所列之發泡醴 係利用一工業用發泡體擠壓機製備。此裝置係為一在通常 之進料、熔化及計量連續區域末端具有兩個額外混合及冷 卻區域之螺旋式壓出機。擠壓機筒在計量與混合區域之間 設有一供發泡劑注入之開口。在冷卻區域之一端附有一具 有一大抵呈四方形開口之模具口型。 一具有約〇.4dg/min之炼體指數(依照ASTM D-1238 ,190°C /2.16 kg)及一 0_922g/cm3之密度的低密度聚乙 唏與一少量之甘油一硬脂酸鹽以一均一之速率一同被進給 本紙張尺度適用中國國家標準(CMS > A4規格(210X297公釐) I —1 . l,f— 1 n ^^1 n^i ._ (請先聞讀背面之注$項再填寫本頁) ----訂. 線 經濟部智慧財產局員工消費合作社印製 26 4 60518 經濟部智慧財產局員工消費合作社印製 五、發明説明(私) 至一擠壓機内。未添加加核劑俾保持大胞室尺寸。擠壓機 中在進給區域係維持於160°c之溫度,在熔化區域係維持 200°C之溫度,在計量區域係維持210°C之溫度,且在混合 區域係維持190°C之溫度。異丁烷以一每一百份聚合物11.8 份(pph )的均一速率被注入至混合區域中。冷卻區域和 模塊之溫度逐漸下降以生成一良好之發泡體。在一 110°C 之冷卻區域溫度和一 108°C之模具溫度下,可得到一密度 約23kg/m3及一大胞室尺寸之實質上閉合胞室發泡體。 厚度約為105mm且寬度約600mm之此一發泡體被保存( PEF1 )且接著被拉伸以減少其厚度至約80mm,且被拉伸 之發泡體亦被保存(PEF2)«藉由拉伸欲將胞室在與垂直 方向成直角的方向上增大。如表1中所示,此拉伸不僅使 擠壓方向之胞室伸長,且亦增加平均胞室尺寸。在與垂直 方向成直角之方向(EH平均)上的大胞室尺寸有助於沖 表1 «U稱 發泡體密度 (kg/m3) 胞室尺寸 播壓 (mm)2 胞室尺寸 垂直 (mm)2 胞室尺寸 擠壓水种均 (mm) 4 胞室尺寸, 三维平均 (mm) 5 PEF1 23 6.2 5.9 5.5 5.7 5.9 PEF2 23 5.8 6.3 6.5 6-4 6.2 PEF3 32 4.9 4,0 4.3 4.2 4-4 PEF4 23 2.9 2.1 2.3 2-2 2.4 PEF5* 40 19 1 .7 1.5 1.6 1.7 -非本發明之一發泡體實例 1依照ASTM D-3756測定之垂直方向胞室尺寸 2依照ASTM D-3756測定之擠壓方向胞室尺寸 3依照A S TM D - 3 7 5 6測定之水平方向胞室尺寸 4在擠壓與水平方向之平均胞室尺寸 5在所有三維度上之平均胞室尺寸 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) ---- n.'i i n* n -- (請先閱讀背面之注意事項再填寫本頁)— ^ Ϋ II 14 A7 460518 V. Description of the Invention (β) ~ Edited in CPPark, Polyolefin Foam, Chapter 9, Handbook of Polymer Foams and Technology. The non-crosslinked foam of the present invention can be extruded by a conventional method. Manufacture of foam shoes. The foam structure is generally formed by heating a thermoplastic polymer resin (ie, a polymer material) to form a plasticized or solution material. The foaming agent is added to form a foamable gel, and the gel The glue is extruded through a die to form a foam product. Prior to mixing with the blowing agent, the polymer material is heated to a temperature above the glass transition temperature or melting point. The blowing agent can be added or mixed into the melt polymer material by any conventional means such as by an extruder, mixer, blender, etc. The blowing agent is raised with the solution polymer And it is enough to avoid the melting of the polymer material under the pressure of substantial foaming and spread the foaming agent evenly. "It is advisable that a nucleating agent can be blended in the polymer melt. Dry blend with polymer material before melting. The foamable gel is typically cooled to a lower temperature to optimize the physical properties of the foam structure. The gel is then squeezed or transported through a mold of a desired shape to a reduced pressure or a lower pressure area to form a foam structure. The lower pressure region is below a pressure maintained by the foamable knee prior to extrusion through the die. The lower pressure may be superatmospheric or subatmospheric (vacuum), but is preferably Atmospheric pressure level. The non-crosslinked foaming system of the present invention is formed in a bonded multi-strand pattern by extruding a thermoplastic polymer resin (i.e., a polymer material) through a multi-port die. The mouth shapes are configured such that contact between adjacent streams of molten extrudate occurs during the foaming process and the contact surfaces adhere to each other with sufficient cohesive force to create a unitary foam structure. Melt extrusion after leaving the mold The paper size is toward the family office (CNS) Α4 (210 X 297 mm) (Please read the precautions on the back before filling out this page} 丨 Packing. Staff of the Central Standards Bureau of the Ministry of Economic Affairs Cooperative Du Yince 15 4 6〇518 A7 B7 Du Yinhua, Central Bureau of Standards, Ministry of Economic Affairs, Consumer Cooperative Production Du 5. Production Description (G) Logistics is in the form of multiple strands or profiles, hoping to be a foam, combination, and Adhering to each other to form a unit structure, according to the desire, the individual strands or profiles to be combined should be maintained to adhere to a unit structure to avoid delamination of the strands during the preparation, forming, and utilization of the foam. Manufacturing combined strand types Apparatus and method for foam construction are taught in US Patent Nos. 3571152 and 4324720, which are incorporated herein by reference. The foam construction can also be formed into a non-crosslinked foam suitable for molding into articles Beads. Foam beads can be prepared by an extrusion process or a batch process. In the extrusion process, a thin strip of foam is produced from a porous strip attached to a conventional foam extrusion device. Foaming In a batch process, individual resin pellets, such as granulated resin pellets, are suspended in a liquid medium that is substantially insoluble, such as water; by blowing a foaming agent in an autoclave or other pressure vessel Introduced into the liquid medium at elevated pressure and temperature and impregnated by the foaming agent; and quickly discharged to atmospheric pressure or a reduced pressure area to foam to form foam beads. This procedure is taught in the text incorporated herein by Reference is made to US Patent Nos. 4379859 and 4444484. The crosslinked foaming system of the present invention is prepared by a crosslinked foaming procedure using a decomposable foaming agent or by a conventional extrusion procedure. When using this A procedure for a cross-linked foam of a decomposable foaming agent 'The cross-linked foam of the present invention may be formed by blending a thermoplastic polymer resin (ie, a' polymer material ') with a decomposable chemical foaming agent to form a The foamable plasticized or melt polymer material is extruded through a mold 1 to cause cross-linking in the melt polymer material, and the melt polymer material is exposed to an elevated temperature to Formed by releasing foaming agent Foam structure. The size of this paper applies Chinese National Standard (CNS) A4 specification (210X 297mm) ~ I order (Please read the precautions on the back before filling this page) 16 460518 A7 -----_ B7 5 2. Description of the invention (/ 4) The material and the chemical foaming agent can be mixed and blended by any conventional device such as an extruder, mixer, blender, etc. Chemical foaming agent It is best to dry blend with the polymer material before the polymer material is heated into a melt form, but it can also be added when the polymer material is in the melt phase. Crosslinking can be caused by adding a crosslinker or by radiation. Coupling and exposure to an elevated temperature to cause foaming or swelling can occur simultaneously or sequentially. If a cross-linking agent is used, it is added in the same manner as chemical foaming agents. In addition, if a cross-linking agent When used, the foamable melt polymer material is heated or exposed to a temperature preferably below 150 ° C to avoid decomposition of the crosslinking agent or blowing agent and avoid premature crosslinking. If radiation coupling is used, the foamable melt polymer material is heated to a temperature preferably below 160 ° C to avoid decomposition of the foaming agent. The foamable melt polymer is extruded or transported through a Shape mold to form a foam structure. The foamable structure is then subjected to an elevated or high temperature (typically 150 ° C -250. (:) such as foaming in an oven to form a foam structure. When the radiation crosslinker is used, it can develop The foam structure is irradiated to cross-link the polymer material, which is foamed at the elevated temperature described above. The structure can be advantageously made in the form of a sheet or a thin strip according to the procedure described above using either a cross-linking agent or radiation. Economy Printed by the Ministry of Standards and Technology Bureau Employee Consumer Cooperatives-i — I, 4i --- I --- 1 __! _ Order (Please read the precautions on the back before filling this page) Except for the application of a decomposable foam The use of a cross-linking agent in the procedure of the cross-linked foam of the agent or the addition of radiation can also be achieved by silane cross-linking as described in cppark, Chapter 9. The cross-linked foam of the present invention can also be A continuous slat structure was made using a long ridge mold as described in GB 2145961A. This patent is incorporated herein by reference. In this procedure, the polymer, decomposable foaming agent is on a paper scale. Applicable to China National Standard (CNS) A4 specification (210 × 297 mm) 17 A7 460518 _____B7 5 Description of the invention (if) ~ and the cross-linking agent are mixed in an extruder; the mixture is heated to cross-link the polymer and the blowing agent is decomposed in a spine mold; and the foam structure is formed and exits The mold is processed, and the contact between the foam structure and the mold is lubricated by an appropriate lubricating material. The cross-linked foam of the present invention can also be formed into parent-linked foam beads suitable for molding objects. Body beads, separated wax particles such as granulated resin pellets are suspended in a liquid medium such as water which is substantially insoluble; a cross-linking agent and a foaming agent under an elevated pressure and temperature in a Soak in an autoclave or other pressure vessel; and quickly vent to atmospheric pressure or a reduced pressure area to expand the foam beads. In another version of this procedure, 'polymer beads are saturated with foaming agent' It is cooled, discharged from the container and then heated by heating or foaming with steam. In a variant of the above procedure, the 'monomer' can be impregnated with the crosslinking agent into the suspended pellet to open> Grafted with a polymer material The foaming agent can be impregnated into the resin pellets when suspended or in a non-aqueous state. The expandable beads are then expanded by heating with steam and by a conventional expandable polystyrene Foam bead molding method. The foam beads can then be formed by any conventional means, such as filling the foam beads into a mold, pressing the shrink mold to compact the beads, and heating the beads. Pellets, such as heating with steam to cause the beads to agglomerate and fuse to form an object. Optionally, the beads can be preheated with air or other blowing agents before charging to the mold. The above procedures and molding methods are excellent Instructions can be found in C p park pp_227-233 'US Patent Nos. 3886100, 3959189, 4168353 and 4429059, all of which are incorporated herein by reference. D Foam Beads can also be used & Zhang Jiao itit Caicajiapi (CNS) Tiege (210X297mm) ---- -18 * (Please read the notes on the back before filling out this page) — Equipment. Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs 460518 Λ7 B7 V. Description of the invention (/ (Public) ~ Prepared by in-appropriate mixing equipment or extruder-polymerization 'Crosslinking agent im ^ it m ϊχ— ^^^ 1 ^^^ 1 .1 ^^^ 1 ^^^ 1 ^^^ 1 ^^^ 1-(谙 Please read the precautions on the back before filling this page ), And a mixture that can decompose the mixture, and the mixture is formed into pellets, and the pellets are heated to crosslink and foam. Another method for making crosslinked foam beads suitable for molding into objects is to melt the polymer material and mix it with a physical foaming agent in a conventional foam extrusion device to form a substantially continuous hair. Thin vesicles. The thin strips of foam are granulated or pelletized to form hair beads. This foam bead can then be coalesced and shaped to form the various objects described above for another foam bead process. Other teachings of this procedure can be found in U.S. Patent No. 3616365 and C_P. Park. Park /? ~, Pp, 224-228, all of which are incorporated herein by reference. In addition, the silane cross-linking technology can be applied in the extrusion process, and the teaching of this process can be found in C.P. Park. SwprflXapter 9 and U.S. Patent No. 4,714,716, both of which are incorporated herein by reference. When the Shibata crosslinking process is used together with a conventional extrusion process, a polymer is grafted with an vinyl functional silane or an azide functional silane and extruded to form a foam. The extruded foam is then exposed to warm, humid air to allow cross-linking to occur gradually. The cross-linked foaming system of the present invention is printed by the Consumers' Cooperative of the Ministry of Economic Affairs of the Ministry of Economic Affairs by mixing polymer materials, a cross-linking agent, and a foaming agent in the form of a foam rubber block to form a thick Block, heating the mixture in a mold enables the cross-linking agent to cross-link the polymer material and the foaming agent to decompose, and expands the foam by releasing pressure in the mold. Alternatively, the raw material of the foam capsule formed when the pressure is released may be reheated to cause further expansion. This paper size applies to China National Standard (CNS) A4 (210X 297 mm) 19 Consumption Cooperation by the Central Bureau of Standards of the Ministry of Economic Affairs of the People's Republic of China 6 Ο 5 1 8 Α7 — _____ Β7__ 5. Description of the invention (/,) Cross-linking polymerization The object sheet is made by irradiating a polymer sheet with a high energy ray or by heating a polymer sheet containing a chemical cross-linking agent. The crosslinked polymer sheet is cut into the desired shape and penetrated with nitrogen under high pressure and at a temperature above the softening point of the polymer. Releasing the pressure causes nucleation of the bubbles and some expansion of the sheet. This sheet is reheated in a low-pressure container at a pressure above the softening point, and the pressure is released to expand the foam. The foam prepared by the above method exhibits a density from about 10 kg / m3 to about 300 kg / m3, has a density of about 15 kg / m3 to about 100 kg / m3, and has a density of about 15 kg / m3 to about 60. A kg / m3 density foam is particularly desirable. In addition, the foam prepared by the above method exhibits an average cell size of about 2mm to 15mm, and a desirable cell size is 2mm to 10mm, more preferably about 3mm to about 10mm, and from about 4mm to about 8mm. It is particularly desirable. In addition, the foam produced by the above method may be an open cell or a closed cell. The foam prepared according to the above method can be used without additional processing steps in sound management. For example, a foam prepared by the above method having an average cell size greater than about 4 mm can exhibit a sufficiently low airflow resistance suitable for use as a sound absorbing material regardless of the properties of other foams, and No additional processing steps are required. Typically, for end users of sound management, less than about 800,000 Rays / m (that is, 800,000 Pa s / m2) is required, depending on the final use of the foam, and less than 400000 Rayls / m (Ie, 400,000 pa s / m2), lower than looooo Ray] s / m (ie, 100,000 pa s / m2), and less than 50,000 Rayls / m (this paper size applies to China National Standards (CNS) A4 specifications (2i〇 X297 mm> n 1------11. I--------> ^ D (Please read the notes on the back before filling out this page) 20 4 60518 A7 B7 V. Invention Explanation (M), ie 50000 Pa s / m2) is more ideal one by one. However, if the basic foam prepared by the above method does not exhibit sufficient sound management properties, 'addition or reinforcement properties such as I) substantially open the cell structure or 2 ) The relatively large connected cell pores' can be granted to the base foam by opening the closed cells in the base foam with mechanical means. Printed by the Consumer Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs, I ----^ 1 2 ^^ 1 ^^ 1 _--m »(Please read the precautions on the back before filling this page) As mentioned earlier, in order to make The foam is effective. The foam should have a structure that substantially opens the cell and a relatively low resistance to air flow. According to the present invention, a foaming system having a substantially open cell structure and a relatively low airflow resistance is prepared by mechanically opening a foam having an average cell size greater than about 2 mm. In most cases, this mechanical opening results in quite large connected cell pores. For example, a closed cell in a foam can be opened by opening a closed cell with a device in a porous thermoplastic polymer foam to open at least some portions or at least one of the base thermoplastic polymer foams. This application of the surface is sufficient to cause some parts of the closed cells in the base polymer foam to be opened. The part of the closed cell that is opened by the mechanical device naturally depends on the scope of application of the device that opens the closed cell. For example, if a small percentage of closed cells are open, the device will be applied to only a portion of the base foam and / or only partially stretch through the thickness of the base foam. However, if a larger percentage of the closed cells are opened, the application of the opening device will be applied to more of the surface of the base foam and / or extend deeper into the thickness of the base foam. The application direction of the device with open and closed cells is not important and can be implemented vertically or in the same direction as the extrusion direction, and can be implemented at any angle relative to the surface of the base foam ° This paper size applies to China National Standard (CNS) A4 (210 X 297 mm) 21 Η π 5 1 8 at __Β7 V. Description of the invention) The means for opening and closing the cell can be any means sufficient to open the closed cell, but the typical method includes perforation, cutting, compression, or combination. Typically, perforation involves piercing the base foam with one or more pointed, sharp objects. Appropriate pointed, sharp objects include needles, punctures, pins, nails, etc. In addition, perforations include shots, laser cutting, high-pressure fluid cutting, gas grabbing, or projectiles. Fig. 1 depicts a cross section of one of the basic foams of the present invention, which is composed of a plurality of closed cells 2. The foams are perforated with a number of pointed, sharp objects 3. In addition, the base foam can be prepared to have elongated cells by stretching the thin strips of foam during expansion. This stretching produces elongated cells without changing, or often increasing cell size in the horizontal direction. Therefore, stretching results in an increased horizontal cell size (Eh average) in a direction perpendicular to the vertical direction and facilitates perforation. Fig. 2 depicts a cross section of a basic foam 1 composed of a plurality of closed cells according to the present invention. The closed cells have been stretched in the pressing direction 4 perforated by a plurality of central heads and sharp objects 3. Fig. 3 is a cross-section of a basic foam according to the present invention composed of a plurality of closed cells. The closed cells have been elongated in the extrusion direction 4 which is perforated by a number of pointed and sharp objects 3 at an oblique angle. Printed by the Central Bureau of Standards, Ministry of Economic Affairs and Consumer Cooperatives.-~ 1 IJ— I-I. II: I (please read the note ^ K on the back before filling this page) The perforation of the basic foam can be any style Perforations, including square and dihedral patterns. In addition, it is desirable that the distance between the perforations is the same as the size of the cells in the vesicles, which penetrates most of the cells. Therefore, when it is desired that most of the cells are perforated, 'the best perforation is caused by one not more than twice the flat diameter of the cells in the basal foam', preferably not more than 15 times, and more preferably equal to the basal foam. The average cell diameter in vivo, and the best one is smaller than the base paper size. Applicable to the Chinese National Standard (CNS) Λ4 specification (210X297). V. Description of the Invention (^) The perforation of the average diameter of the cells in the vesicle is separated from each other by a perforation. Although the choice of a sharp, pointed, object that penetrates the basic foam body depends on many factors, including the average cell size, the desired perforation spacing, etc., can be used to make certain foams of the invention Pointed, sharp objects typically have a diameter of about 1 mm to about 4 mm. Cutting can be performed by any device sufficient to cut through at least a portion of the foam ' and includes a knife, saw, and the like. By cutting, the cells of the basic foam body must be opened only on the cutting surface, leaving the cells inside the foam body unchanged. Therefore, cutting does not reduce the airflow resistance throughout the thickness of the foam. But 'opening the surface cell by cutting is sufficient for some sound management applications, especially if the cell size is large enough and / or leaves uncut foam sufficiently thin. Although not subject to any particular theoretical constraints, the inventors believe that in order to effectively absorb sound, it is not necessary for the entire foam thickness to have low airflow resistance. This is because sound is a pressure wave of air, which is conducted by air molecules moving in a vibratory manner (that is, air molecules moving back and forth at a fixed average position * molecules that collide with adjacent layers of air). The air itself does not move a large distance to the thickness of the foam. Therefore, there is no real spatial flow during the transmission of sound through a foam matrix. However, sound is dissipated by the heat formed when air moves forward and backward, causing friction in one of the cell walls. Since the molecule hits a molecule perpendicular to its direction of motion with a large molecule, a sound wave of a pressure wave passes through a soft film blocking its channel, causing the film to vibrate and in turn causing air vibration on the other side. Therefore, a few layers of the flexible film, such as the foam in which the surface cells of the present invention have been cut, do not change the inner core without excessively damaging the sound absorbing ability of the foam. This paper size applies to China National Standard (CNS) A4 (210X 297 mm) ^^ 1 m. I HI m ^^ 1 ......... I— HI «II 1 ^ 1 (please first Read the notes on the back and fill out this page} 23 A7 60510 ____B7 V. Description of the invention (2 /) Compression as a means of opening the cell can be achieved by any means sufficient to apply external force to one or more surfaces of the foam It will cause the cells in the basic foam to rupture and open. Due to the high pressure difference across the cell wall, the compression during or after perforation will crack the cells adjacent to the channel caused by the perforation. It is especially effective on the wall of the chamber. In addition, unlike pinhole drilling, pressure can cause the cell wall to crack in all directions, causing the tortuous path required for sound absorption. The mechanical opening of the closed cell of the basic foam Reduced airflow resistance of the base foam by large pores in the cell walls and pillars. Regardless of the specific device being implemented, the opening of this closed cell in the base thermoplastic polymer foam can increase Sound absorption, sound insulation, fluid absorption 'And the filtering properties of the foam. Of course, the percentage of cells that are mechanically opened will depend on many factors, including cell size, cell shape, means of opening (ie, perforation, cutting' compression), and application of the opening method to The scope of application of the basic foam, etc. In order to reduce the airflow resistance to the greatest extent, it is better that more than 50% of the closed cells in the basic foam are opened by the above-mentioned mechanical device, more preferably more than 70% ' And the best is greater than 90%. In order to maximize the percentage of mechanically open cells, it is best to use a combination of compression and perforation to open the cells. Figure 4 depicts the invention by many squeezes that have been compressed for the first time. The transverse load-bearing surface of the basic foam body 1 composed of elongated cells in the pressure direction 4 and then when the foam body is compressed, it is perforated with many sharp points and sharp bodies 3. In addition to the previously discussed In addition to adding a flame retardant to the selection of the polymeric material, the foam of the present invention can also be extruded, and it is best to apply the Chinese National Standard (CNS) A4 specification (210X297 mm>) at this paper size- -I -—- I- :--— ^^ 1 ^^ 1---I: (Please read the precautions on the back before filling out this page) Printed by the China Standards Bureau of the Ministry of Economic Affairs and Consumer Cooperatives 24 46〇518 Α7 Β7 Intellectual Property of the Ministry of Economic Affairs Printed by the Bureau ’s Consumer Cooperatives 5. Description of the Invention (z) It has undergone any other processing steps 'such as elongation by stretching and the mechanical opening of the closed cell is impregnated with a flame retardant. When used in sound insulation' The foamed body of the present invention can be used as a core layer in a multilayer sound insulation board, which consists of a cover layer, a foam core layer attached thereto, and a core layer through a long strip , Patches, spots, or other geometrical protrusions (hereinafter generally referred to as contact points) constructed with separate contact points fixed with a 'gap between the core layer and the structure' and at long intervals and / or In the case of thin cladding layers, _ 丨 age I to keep the core layer a certain distance from the structure. The structure in which the core layer is fixed with separate contacts may be a wall or a ceiling or any other suitable structural element. Alternatively, the structure may be a second covering layer. The resulting sandwich panel can be used as a partition element or partition wall. This board can be used in the construction and other industries to improve the sound insulation properties of buildings and / or machinery. Examples of such boards are described in WO 95/14136, published on 1995, 5, 26, the contents of which are incorporated herein by reference reference. When used as a core layer in a multilayer board, the foam of the present invention can be formed into a profile of any type. For example, the foam of the present invention can be formed into a linear cross-section. Fig. 9 depicts a longitudinal section of the present invention made of a foamed body consisting of a foamed core 5 of the linear type, designated I. However, the foam of the present invention can also be made into a longitudinal section showing a low dynamic rigidity. For example, 'the foam of the present invention can be made into a longitudinal section composed of a foam core 5' narrow strips of the same or another foam 6 have been attached to the same end of the foam core 5 Or both ends. The vertical section in Figure 〖〇 is labeled U. In addition, the foam of the present invention can be made of a foam (please read the precautions on the back before filling this page) * 〆4 · 25 4 6051 8 A7 B7 V. Description of the core 5 In longitudinal section, narrow strips of the same or another foam 6 have been attached to the opposite sides of the foam core 5 at intervals and narrow strips of the same or another foam 6 have been attached to the foam. Both sides of the core 5 are opposed to each other at both ends of the foam core 5. The 11th icon is shown as w. When the foamed body of the present invention is made into such a longitudinal facet and placed between the panels, these designs convert the compressive strain on the panel into a pair of foamed straining bending strains. There is a sufficient distance between the false support bars ' This configuration provides the very low dynamic stiffness required. In the example of the longitudinal section W, the distance between the midpoints of the narrow strips 6 on the same side of the foam core 5 is at least 250 mm 'and preferably between about 300 mrn and about 600 mm. In the example of the longitudinal section U, the distance between the midpoints of the narrow strips is at least 350 mm 'and preferably between about 450 mm and 600 mm. The following examples of the foam of the present invention are not to be construed as limiting. Unless otherwise indicated, all percentages' parts and ratios are by weight. Example 1 shows a method for preparing the foam. The foamed cymbals listed in Table 1 were prepared using an industrial foam extruder. This unit is a screw extruder with two additional mixing and cooling zones at the end of the usual continuous feeding, melting and metering zone. The extruder barrel is provided with an opening through which the blowing agent is injected between the metering and mixing area. At one end of the cooling zone, a die opening with a large square opening is attached. A low-density polyethylene glycol with a refinement index of about 0.4 dg / min (according to ASTM D-1238, 190 ° C / 2.16 kg) and a density of 0-922 g / cm3 and a small amount of glycerol monostearate to A uniform rate is fed together. This paper size applies the Chinese national standard (CMS > A4 size (210X297 mm) I — 1.. L, f — 1 n ^^ 1 n ^ i ._ (Please read the back first (Note the item in $, then fill in this page) ---- Order. Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs 26 4 60518 Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs Inside the machine. Nucleating agent is not added to maintain the size of the large cell. In the extruder, the temperature is maintained at 160 ° c in the feeding area, 200 ° C in the melting area, and 210 ° C in the measurement area. The temperature in the mixing zone is maintained at 190 ° C. Isobutane is injected into the mixing zone at a uniform rate of 11.8 parts (pph) per 100 parts of polymer. The temperature of the cooling zone and the module gradually decreases to Produces a good foam. A cooling zone temperature of 110 ° C and a mold temperature of 108 ° C. A substantially closed cell foam having a density of about 23 kg / m3 and a large cell size is obtained. This foam having a thickness of about 105 mm and a width of about 600 mm is stored (PEF1) and then stretched. In order to reduce its thickness to about 80mm, and the stretched foam is also preserved (PEF2) «by stretching the cell to increase the direction at right angles to the vertical direction. As shown in Table 1, This stretching not only elongates the cells in the extrusion direction, but also increases the average cell size. The large cell size in a direction perpendicular to the vertical direction (EH average) helps to punch the table Body density (kg / m3) Cell size seed pressure (mm) 2 Cell size vertical (mm) 2 Cell size squeezed water average (mm) 4 Cell size, three-dimensional average (mm) 5 PEF1 23 6.2 5.9 5.5 5.7 5.9 PEF2 23 5.8 6.3 6.5 6-4 6.2 PEF3 32 4.9 4,0 4.3 4.2 4-4 PEF4 23 2.9 2.1 2.3 2-2 2.4 PEF5 * 40 19 1.1.7 1.5 1.6 1.7-not one of the foams of the present invention Example 1 Cell size in the vertical direction measured in accordance with ASTM D-3756 2 Cell size in the extrusion direction measured in accordance with ASTM D-3756 3 Measured in accordance with AS TM D-3 7 5 6 Cell size in horizontal direction 4 Average cell size in extrusion and horizontal direction 5 Average cell size in all three dimensions This paper size applies Chinese National Standard (CNS) A4 specification (210X 297 mm) ---- n.'iin * n-(Please read the notes on the back before filling this page)

、1T 線 -27 經濟部智慧財產局員工消費合作社印製 60518 A7 B7五、發明説明) 其他列於表1中之聚乙烯發泡體(PEF )係藉如對PEF1 和PEF2所記述之實質上相同程序被製備。每一發泡體製 造之異丁烷含量可變化以達成所需要之密度,且一少量之 成核劑被添加以作胞室尺寸控制。所有的發泡體具有一實 體上閉合胞室構造。 試驗1 沖孔試驗 發泡體被切割成約5 5mm厚度之板塊,且以一預定間 距之正方形圖案在發泡體板塊上沖出孔。在沖出10、5及 4mm間距之孔時,係使用一 2mm直徑之針。3mm間距之孔 係用一具有許多固定在所需圖案上之1.5mm針的沖孔板沖 出。沖孔之程度可便利地以孔密度(即每平方公分之孔數 )表示。以10、5、4和3 mm之正方形圊案沖孔分別造成一 1、4、6.25及11.1孔/ cm2之孔密度。從每一發泡體試樣 中鑽出整個55mra厚度之29mm直徑圓柱形樣本且樣本之敞 開胞室含量係依照ASTM D-2856測定。敞開胞室數據對每 一發泡體樣本與沖孔圖案記載於表2中。 11-.--Ή-----f--------、u------l (請先閲讀背面之注意事項再填寫本頁) 表2 發泡體型態 孔數, 表面開孔2 10mm問距3 5mm間距4 4mm間距5 3mm間距6 PRF1 63 55 84 90 94 95 PRF2 77 59 81 94 95 95 PRF3 ND 41 53 82 87 95 PRF4 ND 23 61 71 78 92 PRF5* ND 18* 30+ 47* 56* 72* ’非本發明之一實例發泡體 1擠壓時發泡體之開孔含量百分比3 ND=未測定 2切割表面胞室體積佔發泡體體積之百分比(依照ASTM D-2856) 3以1 Omm間距穿扎之發泡體開孔含量百分比 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) 28 經濟部智慧財產局員工消費合作社印製 d 605 1 8 μ __B7五、發明説明(在) 4以5mm間距穿孔之發泡體開孔含量百分比 5以4mm間距穿礼之發泡體開孔含量百分比 6以3 m m間距穿孔之發泡饉開孔含量百分比 數據清楚顯示胞室愈大則愈容易以沖孔造成敞開胞室 。為了對大多數的胞至沖孔,孔間距需等於或小於胞室尺 寸。因於沖孔密度愈大成本愈高,一具有較大胞室尺寸之 發泡體較佳。每平方公分沖一孔係為在某些具有<2111111胞 室尺寸之發泡體所商業化實施者。每平方公分沖出超過四 個孔可能並非不可行,但實施上有所困難。此外,一未經 沖孔之巨多孔發泡體(例如PEF1和PEF2 )已有一高含量 之敞開胞室被形成。多數之高敞開胞室含量來自於樣本之 切開表面胞室。例如,PEF2之表面切開胞室相當於發泡 體總共77%之敞開胞室含量中的約59%。 試驗2 壓縮試驗 得自實例1之發泡體PEF 1係先以一 2mm直徑之針沖礼 成一 5mm X 5mm之圖案。沖孔之發泡體具有一約為93.5% 之敞開胞室含量(以ASTM D-2856程序C測定)。一橫載 面11 cm X cm且厚度為7cm之發泡體樣本由發泡體板條中被 切割出且在厚度方向上利用一壓機壓縮至厚度變為5mm。 在壓縮期間,一爆裂聲表示胞室破裂被聽見。發泡體之敞 開胞室含量增加至96.7%,接近發泡體之最大可能敞開胞 室含量(即,〜97% )«明顯地,大部分剩餘之閉合胞室 係藉壓縮而爆開。 (請先鬩讀背面之注意事項再填寫本頁) 4 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐) -29 經濟部智慧財產局員工消費合作社印製 46051 8 五、發明説明(27 ) 試驗3 氣流試驗_ 此一試驗顯示較大的氣流道比在一較小胞室發泡體上 更容易藉由在一較大胞室發泡體上沖孔被造成。使用在此 試驗中之裝置為—相似於ASTM D-3574和ISO 9053 (方法 A)中所敘述之氣流試驗機。其係由一 10 cm内徑,由英斯 萊特試驗儀之激勵而驅動的氣動汽缸活塞,一由7cm内徑 之塑膠管和一蓋所組成之試樣座,一水測壓計和分類連接 管所組成。空氣以一固定速率泵唧通過一裝載在座上的樣 本且通過樣本之壓力降用測壓計測量。 實務上’三個不同胞室尺寸之發泡體在此試驗令被選 用:二個實例1所製備之聚乙烯發泡體,PEF4和PEF5,以 及一聚丙烤發泡體。聚丙婦發泡體為一在一與實例1中者 之結構相同利用一具有多數孔之模具的發泡體擠壓流水線 上製備之具有一的聚結細條發泡體。聚丙烯發泡體(PPF )具有一约〇.4mm之胞室尺寸(3D平均),一接近17 kg/ m3之密度,以及一 84%之敞開胞室含量(ASTM D-2856程 序A ) °發泡體平行於擠壓方向被切成35rnm厚之板塊。一 6.4mm直徑之圓形樣本由板塊中被切出並裝載在試樣座上 。一填隙材料被用來封阻管表面的邊緣。首先,橫越樣本 之壓力降係以一慢空氣速率測定(在相當約丨_ Umm/min 之活塞速度下)以確保邊緣之—適當密封,且測定初生發 泡體的氟流阻力。接著’在發泡體樣本上以一預定直徑之 針沖孔,且一適當流速之壓力降被測定。此程序持續至有 本紙張尺及通州〒罔國參標準(〇灿)人4規格(2丨〇乂297公釐) ·. I- - I ^^1 «^1 I n ^^1 Ϊ —I In41 .. i ,,-——1^1 i In (請先閲讀背面之注意事項再填寫本頁) 30 Α7 Β7 五、發明説明(¾ ) 九個孔被沖出在樣本上為止。每一孔之氣流係由每單位壓 力梯度之氣流間的遞降斜度(壓力降/樣本厚度)以及孔 數計算。以2,3及4 mm之針沖孔的發泡體樣本之氣流數據 以m4/ Gpa s (每十憶帕立方米/每秒米)為單位記於表3 。就一特定針尺寸而言,較大之胞室發泡艘。此外,所有 發泡體均為較大之針比較小之針產生更大之氣流孔。針尺 寸對氣流之效果對一具有較大胞室尺寸之發泡體較大。 (請先閱讀背面之注意事項再填寫本頁) 装. -It 經濟部智慧財產局員工消費合作社印製 試驗4 不同胞室尺寸之發泡體間的氣流阻力與聲音吸收比較 使用在本實例中之裝置為一4206型之聲阻抗管與3555 型信號分析儀,二者皆由Brueel及Kjaer A/ S, Naerum, Denmark供應。此裝置被用來依據ASTM E-1050所記述方 法測定一發泡體之標準聲音吸收系數。實務上,直徑29mm 厚度35mm之樣本從試驗3所使用之樣本中被鑽出。利用一 選定直徑之針在樣本厚度方向上沖出七個孔。此孔約相等 地間隔呈一三角形圖案,其中一孔被沖在中心且其餘被沖 出在一邊9mm之六邊形角落。孔之密度被計算為約1.06孔 線 表3 發泡體型態 氣流 2mm針(m4/Gpa s)1 3 mm針(m4/Gpa s)2 4 mm 針(m4/Gpa s)3 PEF4 0.23 1.0 2.7 PEF5 0.17 0.72 1.2 *PEF 0.17 0.46 0.49 ‘非本發明之一實例 1通過一以一2mm之針穿透發泡趙之孔的空氣流 2通過一以一3mm之針穿透發泡體之孔的空氣流 3通過一以一4mm之針穿透發泡體之孔的空氣流 本紙張尺度適用中國國家標準(CNS ) A4規格(210XM7公釐} 31 460518 五、發明説明(z?) / cm2。具有2,3及4mm直徑之針被使用。無孔之初生發 泡體亦被試驗以供比較。沖孔之發泡體樣本比氣流阻力由 表3所示之每孔氣流計算出。初生發泡體之比氣流阻力被 直接測出。比氣流阻力和聲音吸收系數係摘述於表4中。 表4 (請先閲讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 ‘非本發明之一實例 1用以穿孔之針的尺寸 2以1000 Rayls測定之35mm厚樣本的比氣流阻力 3依照ASTM E-1050測定在一 500Hz之頻率的聲音吸收系數 4依照ASTM E-1050測定在一 1000Hz之頻率的聲音吸收系數 5依照ASTM E-丨050測定在一2000Hz之頻率的聲音吸收系數 6在低於1600Hz之頻率下的最大聲音吸收系數;NE=不存在 7發生最大吸收處之頻率 所有的初生發泡體具有一非常高的比氣流阻力且沖孔使氣 流阻力遽減。同樣地,發泡體胞室愈大且使用的針愈大, 則比氣流阻力減少地更大°初生發泡體吸收聲音不良。十 分清楚地,沖孔發泡體比初生發泡體有更佳的聲音吸收。 試驗型態 發泡體型態 針尺寸 (mm)1 比氣流阻力 (lOOORayls)? 聲音吸收系^ 改 500 Hi 1000 H2^ 2000 Hz5 tA6 頻率 (Hz)7 4.1 PEF4 無 4056 0.11 0‘1 1 0‘16 NE NE 4·2 PEF4 2 14.4 0,42 0.34 0.28 0.50 700 4.3 PEF4 3 3.2 0.31 0.53 0.68 0.75 800 4.4 PEF4 4 1.2 0.29 0.63 0.52 0,83 810 4.5 PEF5 無 4718 0.05 0.06 0.09 NE NE 4.6 PEF5 2 19.4 0.Ϊ3 0.07 0.14 0.16 350 4.7 PEF5 3 4.6 0.29 0.13 0.19 0.30 480 4.8 PEF5 4 2.9 0.32 0.20 0,21 0.33 540 4.9 PEF4 無 2926 0.05 0.06 0.09 NE NE 4.10 PEF4 2 20.0 0.14 0.09 0.11 0.23 280 4,11 PEF4 3 7-2 0.25 0·12 0.15 0.31 350 4.12 PEF4 4 6.7 0.42 0.21 0.18 0.43 580 本紙張尺度適用中國國家標準(CNS ) A4規格(2!0X297公釐) 32; 460518 A7 B7 五、發明説明) 一般而言,比氣流阻力愈小’發泡體所具有之聲音吸收系 數愈大。沖礼發泡體之聲音吸收曲一般看來係如第5圖中 所示,以3mm直徑之針沖孔的發泡體被比較。聲音吸收曲 線在一低於1000Hz之頻率經過最大值,下降且接著在 6400Hz之測量頻率範圍經歷數個峰。由於低於2〇〇〇Hz, 且更重要者,低於1000Hz之聲音吸收特性最為重要,該 等數據被表示於表4和第5圖中。在第5圖中,即便發泡體 樣本以相同之針及相同之孔密度沖孔,大胞室PEF4發泡 體(試驗編號4.3)吸收聲音遠較小胞室PEF5(試驗編號4.7 )及PPF (試驗編號4.11 )為佳。聲音吸收能力之差別不 單單來自比氣流阻之差。例如,以一 4mm之針沖孔的發泡 體PEF4吸音遠比以3mm之針沖孔的發泡體PEF4為差,即 便前者比後者具有較低之比氣流阻力。可從試驗丨演繹出 較大胞室之發泡體似乎比較小胞室發泡體有較大的體積被 沖孔敞開。 試驗5 經濟部智慧財產局員工消費合作社印製 太盒^尺寸之發泡體間的敞開胞室含量虡聲音铒此比鲂 孔間距對聲音吸收和敞開胞室含量的影響在此試驗中被研 究。如實例1中所製備之大胞室發泡體,初生與沖孔者, 係接受試驗4中的聲音吸收試驗。除了長度縮短至約35mm 以外樣本係與實例1中用於敞開胞室試驗者相同。數據摘 記於表5中》 本紙張適财關家料(CNS )从雜(21QX 297公董) 4 60 518 A7 B7 五、發明説明(9/ ) 表5 號 發泡體型態 針間距 (mm)1 開孔含量 聲音吸收系數 500Hz5 1000Hz4 2000Hz5 最大6 頻雜)7 5.1 PEF2 無 77 0.46 0.66 0.58 0.95 730 52 PEF2 10 81 035 0,79 0.72 0.98 S20 53 PEF2 5 84 0.14 0.65 0.69 0.87 1280 54 PEF2 4 95 0.13 0.63 0.61 0.85 1290 5.5 PEF2 3 95 029 0.72 0-69 0.93 1360 5.6 ΡΕΓ3 無 ND 031 0.47 0,49 0.72 730 5.7 PEF3 10 53 0.41 0.52 0.51 0.76 730 5.8 PEF3 5 82 0.17 0.78 052 0.91 1200 5.9 PEK3 4 87 0.18 0.83 0,51 0.93 1140 5.10 PEF3 3 95 0J8 0.94 0.99 0.95 960 5.11 PEF4 10 61 027 0.74 0.44 0.87 850 5A2 PEF4 5 71 022 0.97 0.54 0.99 1060 5」3 PEF4 4 79 0.17 0*84 0.52 0.98 1200 5.14 PEF4 3 92 0.41 0.91 0.80 0.95 880 ND=未測定 無=無穿扎(初生發泡體) 1在一正方形圖案中之孔間距離 2按照ASTMD-2856程序C所測定之開孔含量;與表1中相同之數據 3依照ASTM D· 1050測定在500Hz下之聲音吸收系數 4依照A STM D-1050測定在1000Hz下之聲音吸收系數 5依照A STM D-105 0測定在2000 Η z下之聲音吸收系數 6在低於丨600 Hz下之最大聲音吸收系數 7最大吸生發生處之頻率 (請先鬩讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 所有發泡體顯示有效之聲音吸收能力。令人驚訝地,初生 大胞室發泡體展現優良的聲音吸收能力(試驗編號5.1和 5.6)。這些發泡體與初生PEF4發泡體(試驗編號4.1)的 完整吸收曲線被比較於第6圖中。大胞室發泡體之優越聲 音吸收能力在第6圖中極明顯。在發泡體表面被切開之胞 室被推論係有助於發泡體之傑出聲音吸收性質。在巨多孔 PEF2的例子中,初生發泡體吸收聲音比沖孔發泡體為佳 本紙張尺度適用中國國家標準(CNS ) A4規格(2丨0X297公釐) 34 經濟部智慧財產局員工消费合作社印製 4 6^518 a? B7 五、發明説明(兌) 且聲音吸收能力易因以2mm之針所沖之孔的孔密度増加而 劣化。此一趨勢在第7圖中可更清楚地看見。聲音吸收係 受到敞開胞室含量與比氣流阻力二者的影響。已知一過低 之比氣流阻力對聲音吸收有害。此提供何以聲音吸收隨孔 密度增加而減少的一解釋。具有3mm沖孔之發泡體的一明 顯趨勢逆轉可能係因使用一較小之針(1.5mm直徑)之故 。在PEF3中’以10mm間距沖孔之發泡體樣本提供最佳之 聲音吸收(試驗編號5.7)。在PEF4中,其具一比較小的胞 室尺寸’ 一具有5mm間距之孔的發泡體(試驗編號5.丨2) 吸收聲音稍比孔間距為10mm之發泡體樣本(試驗編號5.11 )為佳° 試驗6 覆面薄膜對聲音吸收之影響 皮層與一附著之薄膜對沖孔PEF2發泡體樣本之影響 在本試驗中被研究。一DAF 899牌之黏膜(由Dow Chemical Company銷售)被使用作發泡體樣本之面層。此薄膜係由 PRIMACORE* 3330 乙烯 / 丙烯酸共聚物(Dow Chemical Company之商標)製備成。此一厚度約為37微米之薄膜被 燙平至一皮層被除去之發泡體樣本表面。熨斗係以襯以一 特氣隆薄片以壁免薄膜黏在贺斗上。二個以lOmm和5min 間距被沖孔之發泡體供本例之試驗使用。以薄膜覆蓋之樣 本與皮層被除去之樣本比較。在發泡體樣本具有以10mm 間距沖孔之例中,試驗包含——皮層留在一面之樣本。所 有樣本的厚度皆固定在35mm且樣本之聲音吸收系數係以 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公嫠) —.Id-------裝--------訂------t (請先閲讀背面之注意事項再填寫本頁) 35 “0518 A7 B7五、發明説明(衫) 具有薄臈或皮層之表面面對聲源而被測定。聲音吸收試驗 之結果記於表6和第8圖,試驗6.4與6.5之結果被比較: 表6 試驗编號 6.1 針間距 ⑴ 10 試樣表面 ⑵ 聲音吸收系數 250 Hz ⑴ 500Hz ⑷ 1000 Hz ⑴ 1600 Hz ⑹ 最大 ⑺ 頻率 ⑴ 去皮 0.09 0.55 0.91 0.41 1.00 】030 6.2 10 有皮 0.19 0.32 0.86 0.31 0.96 920 6.3 10 有薄琪 0.20 0.28 0.84 0.28 0.½ 920 6.4 5 去皮 0.05 0.24 0.59 0.78 0,82 1280 6.5 5 f有薄膜 0.47 0.44 0.72 0.45 0.94 760 1在以mm計之正方形圖案中的孔間距離 (請先閲讀背面之注^^項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 如表與第8圖中所示,薄膜附貼戲劇化地改善了發泡 體在低頻下之聲音吸收性能。在以5mm間距沖孔之發泡體 樣本例中’薄膜提高了整個在1000Hz以下頻率範圍内的 聲音吸收。 試驗7 作為一 W形低剛性縱剖面插入物的聲音吸收性能 本試驗令,沖孔發泡體作為一雙片隔板之性能被研 究《'聲音傳遞試驗係在一CEBTP實驗室中完成。在CEBTP 之聲音傳遞減少設備具有一 55m3體積之源室以及一 51 m3 之接收室。在36cm厚之隔離壁中間設有一從源室觀看為 0.96m寬,1.96m厚並12cm深之開口。此孔在壁厚之其餘 部分擴大為l,08mX2.06m之尺寸。一 l.〇5mX2.05m尺寸之 板被裝設在此開口内。通過該板之聲音傳遞損耗被測定並 依照ISO R7H-1968中所述之方法被計算。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) ~ -1T line-27 Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs 60518 A7 B7 V. Description of the invention) The other polyethylene foams (PEF) listed in Table 1 are substantially the same as those described in PEF1 and PEF2. The same procedure was prepared. The isobutane content of each foaming system can be varied to achieve the required density, and a small amount of nucleating agent is added for cell size control. All foams have a physically closed cell structure. Test 1 Punching test The foam was cut into a plate having a thickness of about 55 mm, and holes were punched out of the foam plate in a square pattern with a predetermined pitch. When punching holes with a pitch of 10, 5, and 4 mm, use a 2 mm diameter needle. The 3 mm pitch holes were punched out with a punching plate having a number of 1.5 mm pins fixed to the desired pattern. The degree of punching can be conveniently expressed in terms of hole density (ie, the number of holes per square centimeter). Punching with square patterns of 10, 5, 4, and 3 mm resulted in a hole density of 1, 4, 6.25, and 11.1 holes / cm2, respectively. From each foam sample, a 29 mm diameter cylindrical sample having a thickness of 55 mra was drilled and the open cell content of the sample was determined in accordance with ASTM D-2856. The open cell data are shown in Table 2 for each foam sample and punch pattern. 11 -.-- Ή ----- f --------, u ------ l (Please read the precautions on the back before filling this page) Table 2 Foam Shape Cells Number, surface opening 2 10mm pitch 3 5mm pitch 4 4mm pitch 5 3mm pitch 6 PRF1 63 55 84 90 94 95 PRF2 77 59 81 94 95 95 PRF3 ND 41 53 82 87 95 PRF4 ND 23 61 71 78 92 PRF5 * ND 18 * 30+ 47 * 56 * 72 * 'Not an example of the present invention Foam 1 The percentage of the open cell content of the foam during extrusion 3 ND = not determined 2 The volume of the cell surface on the cutting surface as a percentage of the volume of the foam (According to ASTM D-2856) 3Percentage of open cell content of foams pierced with a pitch of 1 Omm. This paper size applies the Chinese National Standard (CNS) A4 specification (210X 297 mm). System d 605 1 8 μ __B7 V. Description of the invention (in) 4 Percentage of open cell content of foam at 5mm pitch 5 Percentage of open cell content of foam at 4mm pitch 6 Foam perforated at 3 mm pitch百分比 The percentage of open cell content clearly shows that the larger the cell, the easier it is to open the cell by punching. In order to punch most cells, the hole spacing must be equal to or smaller than the cell size. Since the higher the punching density, the higher the cost, a foam having a larger cell size is preferred. Punching a hole per square centimeter is a commercial practice in certain foams having a cell size of < 2111111. It may not be impossible to punch more than four holes per square centimeter, but it is difficult to implement. In addition, an unpunched macroporous foam (such as PEF1 and PEF2) has been formed with a high content of open cells. Most of the high open cell content comes from the cut surface cells of the sample. For example, the surface cut cell of PEF2 corresponds to about 59% of the total open cell content of 77% of the foam. Test 2 Compression test The foam PEF 1 obtained from Example 1 was first punched into a 5mm X 5mm pattern with a 2mm diameter needle. The punched foam has an open cell content of about 93.5% (determined according to ASTM D-2856 procedure C). A foam sample with a lateral load surface of 11 cm X cm and a thickness of 7 cm was cut from the foam slat and compressed in a thickness direction by a press to a thickness of 5 mm. During compression, a popping sound indicates that a cell rupture was heard. The open cell content of the foam was increased to 96.7%, which was close to the maximum possible open cell content of the foam (ie, ~ 97%) «Obviously, most of the remaining closed cells were burst open by compression. (Please read the precautions on the reverse side before filling out this page) 4 This paper size applies the Chinese National Standard (CNS) Α4 specification (210 × 297 mm) -29 Printed by the Intellectual Property Bureau of the Ministry of Economic Affairs Consumer Cooperatives 46051 8 V. Description of the invention (27) Test 3 Airflow test_ This test shows that larger airflow channels are more easily caused by punching holes in a larger cell foam than on a smaller cell foam. The device used in this test was-similar to the airflow tester described in ASTM D-3574 and ISO 9053 (Method A). It is a pneumatic cylinder piston driven by a 10 cm inner diameter and driven by an Inslet tester, a sample holder composed of a 7 cm inner diameter plastic tube and a cover, a water pressure gauge and a classification connection Composed of tubes. Air is pumped at a fixed rate through a sample mounted on the seat and the pressure drop across the sample is measured with a manometer. Practically, three foams of different cell sizes were selected in this test order: two polyethylene foams prepared in Example 1, PEF4 and PEF5, and a polypropylene roasted foam. The polypropylene foam was a coalesced thin strip foam prepared on a foam extrusion line having the same structure as in Example 1 using a mold having a plurality of holes. Polypropylene foam (PPF) has a cell size (3D average) of about 0.4mm, a density close to 17 kg / m3, and an open cell content of 84% (ASTM D-2856 Procedure A) ° The foam was cut into 35rnm thick plates parallel to the extrusion direction. A circular specimen with a diameter of 6.4 mm is cut out of the plate and loaded on the sample holder. An interstitial material is used to block the edges of the tube surface. First, the pressure drop across the sample is measured at a slow air rate (at a piston speed of approximately 丨 _ Umm / min) to ensure that the edges are properly sealed and the resistance to fluorine flow of the primary bubble is measured. Next, a hole of a predetermined diameter is punched in the foam sample, and a pressure drop at an appropriate flow rate is measured. This process continues until there is a paper ruler and Tongzhou 〒 罔 Ginseng Standard (〇 Chan) person 4 specifications (2 丨 〇 乂 297 mm) ·. I--I ^^ 1 «^ 1 I n ^^ 1 Ϊ — I In41 .. i ,, -—— 1 ^ 1 i In (Please read the notes on the back before filling this page) 30 Α7 Β7 V. Description of the invention (¾) Nine holes are punched out on the sample. The airflow of each hole is calculated from the descending slope (pressure drop / sample thickness) between the airflow per unit pressure gradient and the number of holes. The airflow data of foam samples punched with needles of 2, 3 and 4 mm are shown in Table 3 in units of m4 / Gpa s (per ten megapascal meters per second meter). For a specific needle size, the larger cell foam vessel. In addition, all foams have larger air holes than smaller needles. The effect of pin size on airflow is greater for a foam with a larger cell size. (Please read the precautions on the back before filling out this page). -It is printed by the Intellectual Property Bureau of the Ministry of Economic Affairs and the Consumer Cooperative Print Test. 4 Comparison of airflow resistance and sound absorption between foams with different cell sizes is used in this example. The device is a type 4206 acoustic impedance tube and a type 3555 signal analyzer, both of which are supplied by Brueel and Kjaer A / S, Naerum, Denmark. This device was used to determine the standard sound absorption coefficient of a foam according to the method described in ASTM E-1050. In practice, a sample with a diameter of 29 mm and a thickness of 35 mm was drilled from the sample used in Test 3. Use a needle of a selected diameter to punch seven holes in the thickness direction of the sample. The holes are approximately equally spaced in a triangular pattern, one of which is punched in the center and the remaining punched out in a hexagonal corner of 9mm on one side. The density of the holes is calculated as about 1.06 hole line. Table 3 Foam type airflow 2mm needle (m4 / Gpa s) 1 3 mm needle (m4 / Gpa s) 2 4 mm needle (m4 / Gpa s) 3 PEF4 0.23 1.0 2.7 PEF5 0.17 0.72 1.2 * PEF 0.17 0.46 0.49 'Not one of the examples of the present invention 1 through an air stream that penetrates the hole of the foam Zhao with a 2mm pin 2 through a hole that penetrates the foam with a 3mm needle Air flow 3 through a 4mm pin through the hole of the foam body The paper size applies the Chinese National Standard (CNS) A4 specifications (210XM7 mm) 31 460518 V. Description of the invention (z?) / Cm2 Needles with diameters of 2, 3 and 4mm were used. Primary foams without holes were also tested for comparison. The specific airflow resistance of punched foam samples was calculated from the airflow per hole shown in Table 3. Primary The specific airflow resistance of the foam is directly measured. The specific airflow resistance and sound absorption coefficient are summarized in Table 4. Table 4 (Please read the precautions on the back before filling out this page) Employee Cooperatives, Intellectual Property Bureau, Ministry of Economic Affairs Print 'Not one of the invention Example 1 Dimensions of a needle for perforation 2 Specific gas of a 35 mm thick sample measured at 1000 Rayls Flow resistance 3 Sound absorption coefficient measured at a frequency of 500 Hz according to ASTM E-1050 4 Sound absorption coefficient measured at a frequency of 1000 Hz according to ASTM E-1050 5 Sound absorption measured at a frequency of 2000 Hz according to ASTM E-050 Coefficient 6 is the maximum sound absorption coefficient at a frequency below 1600Hz; NE = There is no frequency 7 where the maximum absorption occurs. All primary foams have a very high specific airflow resistance and punching reduces the airflow resistance. Similarly Ground, the larger the foam cell and the larger the needle used, the greater the reduction of airflow resistance. The primary foam has poor sound absorption. It is very clear that the punched foam is better than the primary foam. Sound absorption. Test type Foam type Needle size (mm) 1 Specific air resistance (lOOORayls)? Sound absorption system ^ Change 500 Hi 1000 H2 ^ 2000 Hz 5 tA6 Frequency (Hz) 7 4.1 PEF4 No 4056 0.11 0 ' 1 1 0'16 NE NE 4.2 PEF4 2 14.4 0,42 0.34 0.28 0.50 700 4.3 PEF4 3 3.2 0.31 0.53 0.68 0.75 800 4.4 PEF4 4 1.2 0.29 0.63 0.52 0,83 810 4.5 PEF5 None 4718 0.05 0.06 0.09 NE NE 4.6 PEF5 2 19.4 0.Ϊ3 0.07 0.14 0. 16 350 4.7 PEF5 3 4.6 0.29 0.13 0.19 0.30 480 4.8 PEF5 4 2.9 0.32 0.20 0,21 0.33 540 4.9 PEF4 None 2926 0.05 0.06 0.09 NE NE 4.10 PEF4 2 20.0 0.14 0.09 0.11 0.23 280 4,11 PEF4 3 7-2 0.25 0 · 12 0.15 0.31 350 4.12 PEF4 4 6.7 0.42 0.21 0.18 0.43 580 This paper size is applicable to Chinese National Standard (CNS) A4 specifications (2! 0X297 mm) 32; 460518 A7 B7 V. Description of the invention) Generally speaking, specific airflow resistance The smaller the foam, the larger the sound absorption coefficient. The sound absorption curve of the punching foam generally appears as shown in Figure 5, and the foam punched with a 3 mm diameter needle is compared. The sound absorption curve passes a maximum at a frequency below 1000 Hz, decreases, and then experiences several peaks at a measurement frequency range of 6400 Hz. Since the sound absorption characteristics below 1000 Hz, and more importantly, below 1000 Hz are the most important, these data are shown in Tables 4 and 5. In Figure 5, even though the foam samples were punched with the same needles and the same pore density, the large cell PEF4 foam (Test No. 4.3) absorbed much less sound than the cell PEF5 (Test No. 4.7) and PPF. (Test No. 4.11) is preferred. The difference in sound absorption capacity is not only due to the difference in specific airflow resistance. For example, a PEF4 foam punched with a 4mm pin is far worse than a PEF4 foam punched with a 3mm pin, even though the former has a lower specific airflow resistance than the latter. It can be deduced from the test that foams with larger cells seem to have a larger volume of punched holes than foams with smaller cells. Experiment 5 The content of open cells between foams printed in the box of the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs 虡 sound: This ratio is the effect of cell spacing on sound absorption and open cell content. . The large cell foams prepared in Example 1 and those born and punched were subjected to the sound absorption test in Test 4. The sample was the same as that used in the open cell tester in Example 1 except that the length was shortened to about 35 mm. The data is summarized in Table 5. "This paper is suitable for household use (CNS) from miscellaneous (21QX 297 public directors) 4 60 518 A7 B7 V. Description of the invention (9 /) Table 5 Foam type needle pitch (mm ) 1 Opening content Sound absorption coefficient 500Hz5 1000Hz4 2000Hz5 Max 6 frequencies) 7 5.1 PEF2 None 77 0.46 0.66 0.58 0.95 730 52 PEF2 10 81 035 0,79 0.72 0.98 S20 53 PEF2 5 84 0.14 0.65 0.69 0.87 1280 54 PEF2 4 95 0.13 0.63 0.61 0.85 1290 5.5 PEF2 3 95 029 0.72 0-69 0.93 1360 5.6 PEF3 without ND 031 0.47 0,49 0.72 730 5.7 PEF3 10 53 0.41 0.52 0.51 0.76 730 5.8 PEF3 5 82 0.17 0.78 052 0.91 1200 5.9 PEK3 4 87 0.18 0.83 0,51 0.93 1140 5.10 PEF3 3 95 0J8 0.94 0.99 0.95 960 5.11 PEF4 10 61 027 0.74 0.44 0.87 850 5A2 PEF4 5 71 022 0.97 0.54 0.99 1060 5``3 PEF4 4 79 0.17 0 * 84 0.52 0.98 1200 5.14 PEF4 3 92 0.41 0.91 0.80 0.95 880 ND = Not determined None = No penetration (primary foam) 1 The distance between the holes in a square pattern 2 The content of open cells measured in accordance with ASTMD-2856 procedure C; same as in Table 1 Data 3 measured at 50 according to ASTM D · 1050 Sound absorption coefficient at 0 Hz 4 Sound absorption coefficient measured at 1000 Hz in accordance with A STM D-1050 5 Sound absorption coefficient measured at 1000 Hz in accordance with A STM D-105 0 Maximum sound at sound absorption coefficient below 2000 Hz Absorption coefficient 7 The frequency at which the maximum absorption occurs (please read the notes on the back before filling out this page). The Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs printed all foams to show effective sound absorption. Surprisingly, the primary large cell foam exhibited excellent sound absorption (Test Nos. 5.1 and 5.6). The complete absorption curves of these foams and the primary PEF4 foam (Test No. 4.1) are compared in Figure 6. The superior sound absorption capacity of the large-cell foam is extremely evident in Figure 6. It is inferred that the cells that were cut on the surface of the foam contribute to the outstanding sound absorption properties of the foam. In the case of the giant porous PEF2, the primary foam absorbs sound better than the punched foam. The paper size is applicable to the Chinese National Standard (CNS) A4 specification (2 丨 0X297 mm). 34 Consumer Cooperatives, Intellectual Property Bureau, Ministry of Economic Affairs Printed 4 6 ^ 518 a? B7 V. Description of the invention (conversion) And the sound absorption capacity is easily deteriorated due to the increase in the hole density of the hole punched with a 2mm needle. This trend can be seen more clearly in Figure 7. The sound absorption system is affected by both the open cell content and the specific airflow resistance. It is known that an excessively low specific airflow resistance is harmful to sound absorption. This provides an explanation of why sound absorption decreases with increasing hole density. A clear reversal of foams with 3mm punched holes may be due to the use of a smaller needle (1.5mm diameter). Samples of the foam punched at 10 mm pitch in PEF3 provided the best sound absorption (Test No. 5.7). In PEF4, it has a relatively small cell size '-a foam with holes of 5mm pitch (test number 5. 丨 2) a sample of foam that absorbs sound slightly more than 10mm of cell pitch (test number 5.11) Better ° Test 6 The effect of a cover film on sound absorption The effect of a skin layer and an attached film on a punched PEF2 foam sample was investigated in this test. A DAF 899 brand of mucosa (sold by the Dow Chemical Company) was used as the top layer for the foam sample. This film is made from PRIMACORE * 3330 ethylene / acrylic copolymer (trademark of Dow Chemical Company). This thin film, about 37 microns thick, was ironed to the surface of a foam sample with the skin removed. The iron is lined with a special air sheet to prevent the wall from sticking to the bucket. Two foams punched at a pitch of 10 mm and 5 min were used for the test of this example. Film-covered samples were compared with samples with cortex removed. In the case where the foam sample has punch holes at a pitch of 10 mm, the test includes a sample with the skin layer left on one side. The thickness of all samples is fixed at 35mm and the sound absorption coefficient of the samples is in accordance with the Chinese National Standard (CNS) A4 specification (210X297 cm) at this paper scale. --Order ------ t (Please read the precautions on the back before filling out this page) 35 "0518 A7 B7 V. Description of invention (shirt) The surface with the thin layer or leather layer is measured against the sound source. The results of the sound absorption test are shown in Table 6 and Figure 8. The results of tests 6.4 and 6.5 are compared: Table 6 Test No. 6.1 Pin pitch ⑴ 10 Surface of the sample 声音 Sound absorption coefficient 250 Hz ⑴ 500Hz ⑷ 1000 Hz ⑴ 1600 Hz ⑹ Maximum ⑴ Frequency ⑴ Tare 0.09 0.55 0.91 0.41 1.00】 030 6.2 10 With skin 0.19 0.32 0.86 0.31 0.96 920 6.3 10 With Poki 0.20 0.28 0.84 0.28 0.½ 920 6.4 5 Peel 0.05 0.24 0.59 0.78 0,82 1280 6.5 5 f with film 0.47 0.44 0.72 0.45 0.94 760 1 Distance between holes in a square pattern in mm (please read the note on the back ^^ before filling this page) Intellectual Property Bureau of the Ministry of Economic Affairs Consumer Cooperatives printed as table As shown in Figure 8, film adhesion has dramatically improved The sound absorption performance of the foam at low frequencies. In the foam sample punched at a pitch of 5mm, the 'film improves the sound absorption in the entire frequency range below 1000Hz. Test 7 was inserted as a W-shaped low-rigid longitudinal profile. Sound absorption performance of materials This test order, the performance of punched foam as a two-piece separator was studied. "The sound transmission test was completed in a CEBTP laboratory. The sound transmission reduction equipment in CEBTP has a volume of 55m3. Source room and a 51 m3 receiving room. In the middle of the 36cm thick partition wall, there is an opening 0.96m wide, 1.96m thick and 12cm deep viewed from the source room. This hole is enlarged to l, 08mX2 in the rest of the wall thickness .06m size. A 1.05m × 2.05m size board is installed in this opening. The sound transmission loss through the board is measured and calculated in accordance with the method described in ISO R7H-1968. This paper size applies China National Standard (CNS) A4 specification (210X297 mm) ~-

A60518 五、發明說明(兴 並依照ISO R 717-1968中所述之方法被計算。 實務上,在實例1十所製備之大胞室聚乙烯發泡體 以一選定之孔圖案用一選定之針沖孔如表7所示。一隔音 聚氨酯發泡體亦被包含在此試驗中以供比較,發泡體被製 成一低剛性結構(W)之縱剖面,如於表6之附註部分所 示。一平直插入物(I )亦就一發泡體被試驗以作比較》13麵 厚之壓製木板被使用作本實例中所有板之面層。壁與樣本 邊緣之間的周圍間隙以一纖維玻璃填充並繼以一填陳材料 密封 表7 編號 發泡體型 態 結構 穿孔_ 5RI (dB ⑷) 針尺寸 (而1) 2 (mu)3 7.1 PEFZ Μ 3 F 94 42.2 7.Z PET2 W 1 Β 9'4 42.6 7.3 PEF2 W 1 ΓΟ 81 40.3 7.4 PEI·^ w 4 5 ΤΓ 40.6 7.5 PEF3 w 3 F - /4 41.2 7.6 FEF3 w έ-- Β 3Ζ 40.0 7.7 ΡΓΓί w 3 -- 67 40.9 7.8 PEF4 w 1 η 40 .Ζ /.y PEF4 u 4 Ιΐ5-- bb 39.1 7.10 PEF4 w ό ID 5ϋ 38.5~~"" 7.11 PEF4 w 1 κτ~— 52 37.6 7ΛΖΧ Pthb w 4 ID 0/ 36.6 7.13* PUF w 無 9b 7.141 PEF2 1 ι 5~- 94 3ΤΓ2 *非本發明之一實例 4 =以一被40闇寬並7關厚之間隔337mm條片(片同側之* 戏間的 距離),其反侧間隔地接胡刮刀(見FIG.U)支^^之發核 心插入 I =具有54mm厚度之直平板核心(見FIG.9) 2用來刺穿以毫米計之扎之針的直徑 3在一以毫米計之正方形圈案中所穿之扎間的距離 t以一 8权形直徑長度35_之試片按照ASTM 〇.2856程序c所測 定之開孔百分比含重’ 5在CEBTP處測定之以分貝計聲音減少指數(A) 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公笼) : U 裝-------I l· ---------^ . (請先閲讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 460518 五、發明説明(芬) 通過板之聲音傳遞損耗數據係以一噪音之A_加權聲 音減少指數被摘記。數據係以胞室尺寸、針尺寸以及孔密 度之一般次序排列。檢視數據顯示衝擊隔音性能之參數有 .插入物結構;發泡體型態;敞開胞室含量;以及氣流阻 力(孔密度和針之尺寸)。低剛性核心結構(w)比平直 者(I)提供一遠較為佳之隔音(比較試驗7_2和7.14)。在 具有W結構之沖孔發泡體之間,敞開胞室含量對於隔音有 最大之衝擊而其次是氣流阻力。被沖孔而具有大於9〇%之 敞開胞室之PEF2發泡體縱剖面提供一介於43-43 dB (A) 之間的聲音減少指數(SRI )。雖然稍低於—聚氨酯發泡 體者’仍相當令人滿意。含有67-82%敞開胞室之由PEF2 ,PEF3和PEF4所製成之發泡體樣本呈現一在4〇〇_412 dB (A )範圍中之SRI =>以一 1 〇mm X 10mm圖案沖孔之PEF4 樣本具有一 52-55 %之敞開胞室含量以及一在37.6至39.1 dB (A)範圍内之界SRI。其中,一以大針沖孔之樣本 產生較大的隔音性能。小胞室PEF5記錄--不令人滿意 之36.6 dB ( A)性能。 試驗8 作為一 U形低剛性縱剖面插入物的聲音吸收性能 在本試驗中,用一2mm之針以一 5mmXmm圖案沖孔 之PEF2發泡體被切割成一不同的低剛性發泡體縱剖面如 表8之附註中所示’且以一雙片板之插入物被試驗。結構 (U )由一 42mm厚之平直發泡體板塊,其在兩端有40min 寬及7mm厚之支柱。U形發泡體核心之隔音性能係藉試驗 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) (請先閱讀背面之注意事項再填寫本頁) -裝· 、11 經濟部智慧財產局員工消費合作社印製 38 & 60518 A7 ______B7 _ 五、發明説明(私) 6中之相同程序被試驗。數據摘記於表8中。 表8 試驗編號 發泡體型態 結構 穿孔 開孔含量 (%) SRI 針尺寸 (mm^ 孔間距 (mm)3 8.1 PEF2 U 2 5 94 43.0 1具有如FIG.10所示形狀之l.〇5m寬插入物,具有—厚度42〇1111之發泡體本體和兩端處 之40mm寬、7mm厚支柱 八η ^ 2用來刺穿以毫米計之孔的釺直徑 3在一以毫米計之正方形圖案中穿孔間的距離 4以一直徑45mm、長度35mm之圓枉形試片按胪ASTM D_2856程序c測定之開孔百分 比含量 5於CEBTP處所測得之聲音減少指數 如同所示,被沖孔之巨多孔發泡體當以一 U形縱刹面 插在一雙片板中時提供一令一滿意之隔音性能。 試驗9 吸水性 一 12cm X丨2cm X 3,5cm之樣本被由試驗8中所使用之 沖孔聚氨酯發泡體中切割出且浸沒在一普通自來水中約30 秒鐘。此樣本由水中被取出且在表面水滴乾之後被稱重° 經發現此樣本比在吸水之前的樣本重1〇·5倍。水巧以容易 經濟部智慧財產局員工消費合作社印製 地由樣本中被擠出。試驗結果指出此一沖孔大多細胞狀發 泡體可被用來製造需要吸水之材料諸如用在一清潔勢令° 試驗10 阻燃浸清 約3 1 cm X 53cm X 1 _25cm之發泡體樣本係由5式驗8 _戶斤 使用之沖孔發泡體製成。一 30%之水溶液由挪威tN〇rfire AS所提供之阻燃材料製備成。適合的阻燃劑含有12-15% 本紙張尺度適用中國國家榡準(CNiS ) a4規格(210X297公釐) 39 A7 460518 B7 五、發明説明(π ) 硫酸銨,1 -4 %之各別四硼酸鈉十水合物,氣化鈉及磷酸 鈉。實務上,一發泡體樣本被浸在被容納於一淺盤中的阻 燃劑溶液中。發泡體樣本被觀察到迅速地吸收阻燃劑溶液 。當由溶液中被取出時,樣本保留大部分所吸收之溶液。 在試驗編號10.3中,溶液自發泡體樣本被擠出。浸透溶液 之樣本被稱重,在一周圍溫度下乾燥四小時,接著在一維 持在60°C之烘箱内隔夜。發泡體樣本之重量在乾燥期間被 監測。在試驗編號10.2和10.3中,鬆散地懸在發泡體樣本 表面上之阻燃劑結晶被被刮除且發泡體中最後保留的阻燃 劑被測定。發泡體樣本接受一項極限氧指數(LOI)試驗 如表9中所示,發泡體樣本吸收大量的溶液且水相對容 易地從敞開胞室發泡體中乾涸。溶液已被擠出之樣本(試 驗編號10.3)顯示在6小時乾燥期間(4小時在周圍溫度下 且2小時在60°C )喪失了大部分所吸收之水。以阻燃劑浸 透之發泡體展現相當高的LOIs。 試驗編號 擠壓否? 重量增加 乾燥後之增加重量 最後FR含量 LOJ (%) 周圍 4 h(g)3 @60°C 2h(g)4 @60°C 4h(g)5 @60°C 16hfe)6 10.1 非 13.5 7.7 4.2 32 2.6 2.6 >31 10.210.3 非 12.7 6.0 3.8 2.9 2.3 1.1 23.5 是 4.0 1.8 1.2 ].) 1.0 0.7 22.3 1非=溶液未被擠出:是=溶液在作用後被擠出 2—克發泡體t被吸收之溶液量 3在周圍溫度下乾燥4小時後在一克發泡體中所餘留之溶液量 4在60Ϊ下乾燥2小時後在一克發泡體中餘留之溶液量 5在60°C下乾燥4小時後在一克發泡體中餘留之溶液量 6在60°C下乾燥丨6小時後在一克發泡體中餘留之溶液量 7在刮去後留在一克發泡體t之固體阻燃劑最終量 8極限氧指數:在一氧與氮之混合物中正好能支持一材料於此試驗條在下在室溫時起 始發火焰燃燒的氣最低濃度,以體積百分比表示 本紙張尺度適用中國國家標隼(CNS) A4規格(210X297公釐) _, 2 ^ m 裝 , J訂^ (請先閱讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 -40 經濟部智慧財產局員工消費合作社印製 A60518 A7 A7 _ B7 五、發明説明) 實例2 本實例中所使用之裝置係一具有與實例i中所使用者 相同結構之工業發泡體壓出流水線a在本實例令,三個另 外的巨多孔聚烯烴發泡體係由一低密度聚乙烯樹脂和一樹 脂與一乙烯-笨乙烯共聚體(ESI)摻合物所製備成。聚乙 烯樹脂具有一 1.8 dg/min (在190°C /2.16 kg下)之熔體 指數及一 0.923 g/cm3之密度。所使用之ESI樹脂為d〇w Chemical Company利用一受限幾何形狀催化劑所製造之 INDEX DS 201品牌。约70/30之苯乙烯/乙烯共聚物樹 脂具有一熔體指數(在19〇。〇/2.16 kg下)為1.1。發泡體 係由一 70/30之聚乙烯樹脂與ES共聚物樹脂之摻合物, 以及聚乙烯所製備。 發泡體膨脹程序實質上與實例1者相同。本實例中所 製備之發泡體列於表10中。異丁烷以9.13 pph之量被使用 作製備所有發泡體之發泡劑。如同在實例1中,一少量之 甘油一硬脂酸被添加用來控制發泡體尺寸穩定度《就聚乙 烯發泡體(PEF6)和ESF1 PE/ESI摻合物發泡體之製備 而言’一少量滑石以一濃縮形式(在同一聚乙烯中有50% 之滑石)被加入以作胞室尺寸控制之用^ PEF6發泡體之 有效滑石含量為0.068 pph且ESF1為0.034 pph。 ESF丨和E.SF2發泡體二者皆係從相同的聚乙烯和ESI樹 脂摻合物製備成。一少量(〇.〇5pph )之抗氡化劑(Ceba GeigyCorp.之IrganoxlOlO)被加入至全部三種發泡體中 。在一约uo°c之冷卻區域溫度與lire之模具溫度下,三 本紙張尺度適用中國國家標準(CNS〉A4規格(210X297公釐) —^n f - - - - - 1 I— ^^—^1 —1— ^^^1 ^—I nn Έ - ^^^1 ^^^1n^i ml ^^^1 (請先聞讀背面之注意事項再填寫本頁) 41 460518 - 五、發明説明) 種配方皆製造成優良品質之發泡體。發泡體之橫截面尺寸 厚度約為60mm且寬度約為620mm。如表1〇所示,發泡體 具有約29-30 kg/m3之密度及大胞室尺寸。平均胞室尺寸 範圍係為5.6至6.7mm。 表10 發泡體名稱 發泡體密度 (kg/m3) 胞室尺寸 垂直 (mm) 胞室尺寸 擠出 (mm) 胞室尺寸 水平 (mm) 胞室尺寸 擠出水平 平均(mm) 胞室 3D平均 (mm ) PEF6 30 7.4 6.0 6.8 6.4 6.7 ESF1 29 5.8 6.0 4.9 5.5 5.6 ESF2 29 6.8 6.8 6.0 6.4 6.5 註: (】)至(5)=與表1令相同 試驗11 藉由沖孔和壓縮而形成敞開胞室 經濟部智慧財產局員工消費合作社印製 發泡體被削成35mm之板塊且用一 2mm直徑之針以 10mm和5mm之間距沖孔。45mm直徑之圓柱形樣本從板塊 中被鑽出。一個有5tnm孔間距之樣本被壓縮成其厚度之95 %並進一步形成敞開胞室。所有的壓縮發泡體恢復成接近 其原始厚度。利用45mm直徑並35mm厚之圓柱形樣本測定 敞開胞室。敞開胞室含量依照ASTM D-2856程序C測定。 如表11所示,所期望之高敞開胞室含量可藉由沖孔被形成 。由於5mm間距之沖孔已經提供92至95%範圍内之敞開胞 室含量,藉由壓縮所進一步形成之敞開胞室少。如同所預 見者’具有稍小於其餘者之胞室的ESF丨形成稍微較少的 敞開胞室。 本紙張尺度適用中國國家棹準(CNS ) A4規格(210X297公釐) 42 460518 A7 B7五、發明説明(4叫 表11 發泡體名稱 10mm間距 ⑴ 5mm間距 ⑵ 5mm間距&壓縮 ⑴ PEF6 72.5 94.7 95.3 ESF1 69.2 92.6 94.5 ESF2 72.9 94.4 95.7 註:所有的開孔含量皆係依照ASTMD-2856程序C測定 (1) 以10mm間距穿孔之發泡體的開孔含量百分比 (2) 以5mm間距穿孔之發泡體的開孔含量百分比 (3 )以10mm間距穿孔且接著壓縮成原始厚度之95%之發泡體的開礼含量百分比 經濟部智慧財產局員工消費合作社印製 試驗12 機械及減震性質 沖孔發泡體之機械及減震性質被測定俾得知發泡體材 料在一夾層板中使用作一插入物之適用性。動態剛性度與 損耗因數係用一振動平台測定。一直徑‘1 〇cm厚度35cm之 圓盤形發泡體樣本被安裝在一振動平台上。在樣本之頂部 載有一相同直徑之顆粒圓形碎料板。碎料板之表面重量約 1 〇 kg/ m3。一加速計被附裝在平台下且另一加速計被附 裝在碎料板載重之頂面上。平台以隨機頻率垂直震動且阻 尼比係由加速計信號利用一試驗4中所使用之Brueel and Kjaer型號3 55 5之信號分析儀測定。動態剛性度係從共振 頻率計算出’且損耗因數從阻尼比計算出。發泡體之機械 和振動性質係列於表12。 JI1---Ί----裝---,--Ί 訂------免'·, . (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度適用中gig!家網^ ( cNS >八4顯_ (2jQx297公着) -43 - A7 B7 5051 8 五、發明説明(4/ ) 表12 發泡體名稱 針間距 (1) 壓縮強度 ⑵ 壓縮模量 (3) 抗張強度 h (4) 抗張模量 (5) 拉伸長度 (6) 動態剛性度 ⑺ 損耗因數 PEF6 10 25 747 154 1260 30 3.5 0.43 PEF6 5 22 566 ND ND ND 1.7 035 ESF1 10 17 482 131 790 51 4.8 0.46 ESF1 5 15 362 ND ND ND 3.2 0.48 ESF2 10 16 464 134 814 54 5.0 0.39 ESF2 5 14 332 ND ND ND 3.1 0.46 經濟部智慧財產局員工消費合作社印製 註:ND=来測定 (1) 以毫米計之正方形圃案中的孔間距離 (2) 依照ASTMD-3575測定之以千帕計垂直方向壓縮強度 (3 )依照ASTM D-3575測定之以千帕計垂直方向壓縮模量 (4) 依照A S T M D -3 5 7 5測定之以千帕計垂直方向於斷裂處之抗張強度 (5) 依照ASTM D-3575測定之以千帕計垂直方向抗張模量 (6) 依照ASTM C-3575測定在垂直方向之拉伸長度百分比 (7) 以一35mm厚,具一每平方米10之表面重量之發泡體試片測定之每立方米兆牛 頓動態剛性度 (8) 在與測定動態剛性度相同條件下測得之損耗因數 如表所示,發泡體具有使用作一夾層板插入物之適當壓縮 強度與抗拉韌度。如同所預期者,在ESI樹脂中之摻合使 得發泡體較軟。PE/ESI摻合物發泡體由其較大的伸長度 顯示係較強韌者。一 5mm間距之較高密度沖孔造成壓縮強 度一少量減少。較高之沖孔密度被證明對動態剛性度有較 大的衝擊。有利地,動態剛性度比壓縮強度有較大程度之 減少。所有的發泡體屐現出0.354至0.48範圍内之低損耗 因數之良好阻尼特性。如同對高阻尼ESI樹脂所期待者, PE/ESI摻合物發泡體一般而言具有比PE發泡體為高之損 耗因數,但在10mm間距孔之發泡體間其差別較小。令人 感到興趣地,PE/ ESI掺合物發泡體於沖孔較多時觀察到 一損耗因數之有利增加。相反地,PE發泡體於沖礼較多 時則經歷一損耗因數之減少。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) ----------裝---.--1 訂------喋 - - - (請先閱讀背面之注意事項再填寫本頁) 44 經濟部智慧財產局員工消費合作社印製 a 605 1 B A7 B7 五、發明説明) 試驗13 聲音吸收系數 沖孔巨多孔發泡體之聲音吸收系數係依照ASTM E 1050利用試驗4中所述之裝置被測定。如表13中所示,聚 合物組成對發泡體之聲音吸收能力具有一微小的影響。如 同前面所觀察到,一高孔密度劣化聲音吸收能力。一巨多 孔發泡體之良好聲音吸收性能再次藉由沖有10mm間距之 孔的發泡體被證實。 表13 發泡體名稱 針間距 (1) 聲音吸收系數 250 Hz (2) 500 Hz (3) 1000 Hz (4) 2000 Hz (5) 最大 (6) 頻率(Hz) (7) PEF6 10 0.21 0.77 0.60 0.75 LOO 800 ESF1 10 0.16 0.79 0.46 0.61 0,92 740 ESF2 10 0.15 0,77 0.50 0,64 0.95 780 PEF6 5 0.08 0.28 0.96 0.43 0,99 960 ESF1 5 0.09 0,29 0.96 0.67 0.98 1020 ESF2 5 0.08 0.25 0,96 0.59 0.99 1030 , 註: (1) 以毫米計之正方形圖案中的孔間距離 (2) 依照ASTM E-1050測定於一250 Hz頻率時之聲音吸收系數 (3 )依照ASTM E-丨050測定於一 500 Hz頻率時之聲音吸收系數 (4 )依照ASTM E-1050測定於一1000 Hz頻率時之聲音吸收系數 (5) 依照ASTM E-1050測定於一2000 Hz頻率時之聲音吸收系數 (6) 在低於1600 Hz之頻率下的最大聲音吸收系數 (7) 最大值發生處的頻率 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) J—1 — Ί----裝---.--Ί 訂------嗲 ·-, (請先閲讀背面之注意事項再填寫本頁) 45 460518 A7 B7 ,F Z修正 年月日 五、發明說明(43 ) 元件標號對照表 1 發泡體 2 閉合胞室 3 銳利物體 4 擠·壓方向 5 發泡體核心 6 發泡體 —,----.--------.裝----^-----訂---------線- (請先閱讀背面之生意事項再填窝本頁) 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐)A60518 V. Description of the invention (calculated according to the method described in ISO R 717-1968. In practice, the large cell polyethylene foam prepared in Example 10 uses a selected cell pattern with a selected cell pattern. The pin punching is shown in Table 7. A sound-insulating polyurethane foam was also included in this test for comparison. The foam was made into a longitudinal section with a low rigidity (W), as shown in the note to Table 6. As shown. A straight insert (I) was also tested for comparison with a foam. 13-face-thick pressed wood boards were used as the facing for all boards in this example. The peripheral gap between the wall and the edge of the sample Filled with a fiberglass and then sealed with a filler material. Table 7 No. Foam type structure perforation_ 5RI (dB ⑷) Needle size (and 1) 2 (mu) 3 7.1 PEFZ Μ 3 F 94 42.2 7.Z PET2 W 1 Β 9'4 42.6 7.3 PEF2 W 1 ΓΟ 81 40.3 7.4 PEI · ^ w 4 5 ΤΓ 40.6 7.5 PEF3 w 3 F-/ 4 41.2 7.6 FEF3 w ---- Β 3Z 40.0 7.7 ΡΓΓί w 3-67 40.9 7.8 PEF4 w 1 η 40 .Z /.y PEF4 u 4 Ιΐ5-- bb 39.1 7.10 PEF4 w ό ID 5ϋ 38.5 ~~ " " 7.11 PEF4 w 1 κτ ~ — 52 37.6 7 Λ ×× Pthb w 4 ID 0 / 36.6 7.13 * PUF w None 9b 7.141 PEF2 1 ι 5 ~-94 3ΤΓ2 * Not one of the examples of the present invention 4 = 337mm strips with an interval of 40 dark widths and 7 close thicknesses (The distance between the movies on the same side of the film), the opposite side is connected with a hair scraper (see FIG.U) at intervals, and the hair core is inserted I = a straight flat core with a thickness of 54mm (see FIG. 9) 2 is used to Pierce a needle with a diameter of 3 millimeters in diameter. A distance t between the ties in a square circle of millimeters is a test piece with an 8-weight diameter and a length of 35 mm. Determining the percentage of openings containing weight '5 Sound reduction index in decibels measured at CEBTP (A) This paper size applies to China National Standard (CNS) A4 specifications (210 X 297 male cages): U Pack ----- --I l · --------- ^. (Please read the notes on the back before filling out this page) Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs 460518 V. Invention Description (Finnish) The sound transmission loss data is noted with an A-weighted sound reduction index of noise. The data are arranged in the general order of cell size, needle size, and hole density. Examining the data shows that the parameters of impact sound insulation are: insert structure; foam type; open cell content; and airflow resistance (pore density and needle size). The low-rigidity core structure (w) provides a much better sound insulation than the straight (I) (Comparative Tests 7_2 and 7.14). Among the perforated foams with W structure, the open cell content has the greatest impact on sound insulation, followed by airflow resistance. The longitudinal section of the PEF2 foam that is punched with more than 90% open cells provides a sound reduction index (SRI) between 43-43 dB (A). Although slightly lower than-polyurethane foam 'is still quite satisfactory. Samples of foams made of PEF2, PEF3, and PEF4 containing 67-82% open cells showed an SRI in the range of 400-412 dB (A) => with a pattern of 10 mm X 10mm The punched PEF4 sample has an open cell content of 52-55% and a bounded SRI in the range of 37.6 to 39.1 dB (A). Among them, a sample punched with a large needle produced greater sound insulation performance. Cellular PEF5 record-unsatisfactory 36.6 dB (A) performance. Test 8 Sound absorption performance as a U-shaped low-rigidity longitudinal section insert In this test, a PEF2 foam punched with a 2mm needle in a 5mmXmm pattern was cut into a different low-rigidity foam longitudinal section such as It is shown in the note to Table 8 and tested with a two-piece plate insert. The structure (U) consists of a 42mm thick flat foam plate with 40min wide and 7mm thick pillars at both ends. The sound insulation performance of the U-shaped foam core is based on the test. This paper size applies the Chinese National Standard (CNS) A4 specification (210X297 mm) (please read the precautions on the back before filling this page). Printed by the Consumer Affairs Cooperative of the Property Bureau 38 & 60518 A7 ______B7 _ 5. The same procedure as in the description of the invention (private) 6 was tested. Data are summarized in Table 8. Table 8 Test No. Foam Type Structure Perforation Opening Content (%) SRI Needle Size (mm ^ Hole Pitch (mm) 3 8.1 PEF2 U 2 5 94 43.0 1 has a shape of 1.05 m as shown in FIG. 10 A wide insert with a foam body with a thickness of 4201111 and a 40mm wide, 7mm thick support at both ends. Eight ^^ 2 diameter used to pierce holes in millimeters 3 in a square in millimeters The distance between the perforations in the pattern 4 is a circular 枉 -shaped test piece with a diameter of 45mm and a length of 35mm. The percentage percentage of openings measured according to 胪 ASTM D_2856 procedure c. 5 The sound reduction index measured at CEBTP is as shown. The macroporous foam provides a satisfactory sound insulation performance when inserted into a two-piece plate with a U-shaped longitudinal brake surface. Test 9 Water absorption-12cm X 2cm X 3,5cm samples were tested in Test 8 The punched polyurethane foam used was cut out and immersed in ordinary tap water for about 30 seconds. This sample was taken out of the water and weighed after the surface was dried. ° It was found that this sample was better than the sample before water absorption 10.5 times heavier. Shuiqiao makes it easier for employees of the Intellectual Property Bureau of the Ministry of Economic Affairs to consume It was extruded from the sample printed by the company. The test results indicate that most of the cellular foams in this punched hole can be used to make materials that require water absorption, such as used in a cleaning potential ° test 10 flame retardant leaching about 3 1 cm X 53cm X 1 _25cm foam samples are made of punched foam used in Type 5 test 8 _ household weight. A 30% aqueous solution is prepared from flame retardant materials provided by tNorfire AS, Norway. 。 Suitable flame retardant contains 12-15% This paper size is applicable to China National Standard (CNiS) a4 specification (210X297 mm) 39 A7 460518 B7 V. Description of the invention (π) Ammonium sulfate, 1-4% each Sodium tetraborate decahydrate, sodium gasification, and sodium phosphate. In practice, a foam sample was immersed in a flame retardant solution contained in a shallow dish. The foam sample was observed to rapidly absorb resistance Fuel solution. When removed from the solution, the sample retains most of the absorbed solution. In test number 10.3, the solution was extruded from the foam sample. The sample saturated with the solution was weighed and dried at an ambient temperature. Four hours, followed by overnight in an oven maintained at 60 ° C. The weight of the foam sample was monitored during drying. In test numbers 10.2 and 10.3, the flame retardant crystals loosely suspended on the surface of the foam sample were scraped off and the last flame retardant remaining in the foam was removed. Measurement. Foam samples were subjected to a Limiting Oxygen Index (LOI) test as shown in Table 9. The foam samples absorbed a large amount of solution and water dried out from the open cell foam relatively easily. The solution was squeezed The sample taken (test number 10.3) showed that most of the absorbed water was lost during the 6-hour drying period (4 hours at ambient temperature and 2 hours at 60 ° C). Flame retardant-impregnated foams exhibit fairly high LOIs. Test No. Extrusion? Weight increase after drying Weight increase last FR content LOJ (%) Around 4 h (g) 3 @ 60 ° C 2h (g) 4 @ 60 ° C 4h (g) 5 @ 60 ° C 16hfe) 6 10.1 Non 13.5 7.7 4.2 32 2.6 2.6 > 31 10.210.3 Non 12.7 6.0 3.8 2.9 2.3 1.1 23.5 Yes 4.0 1.8 1.2].) 1.0 0.7 22.3 1 Non = solution is not squeezed out: Yes = solution is squeezed out after action 2-grams of hair Amount of solution absorbed by foam t 3 Amount of solution remaining in one gram of foam after drying at ambient temperature for 4 hours 4 Amount of solution remaining in one gram of foam after drying at 60 ° C for 2 hours 5 The amount of solution remaining in one gram of foam after drying at 60 ° C for 4 hours 6 The amount of solution remaining in one gram of foam after drying at 60 ° C for 6 hours 7 After scraping off Final amount of solid flame retardant left in one gram of foam t. Limiting oxygen index 8: A mixture of oxygen and nitrogen can just support a material. At this temperature, the test strip has the lowest initiation of flame combustion at room temperature. Concentration, expressed in percent by volume. This paper's dimensions are applicable to China National Standard (CNS) A4 (210X297 mm) _, 2 ^ m pack, J order ^ (Please read the precautions on the back before (Write this page) Printed by the Employees 'Cooperatives of the Intellectual Property Bureau of the Ministry of Economics-40 Printed by the Employees' Cooperatives of the Intellectual Property Bureau of the Ministry of Economics A60518 A7 A7 _ B7 V. Description of the Invention) Example 2 The device used in this example is an example The industrial foam extrusion line of the same structure used by i in the example a. In this example, three additional macroporous polyolefin foaming systems are composed of a low density polyethylene resin and a resin and an ethylene-stupid ethylene copolymer. (ESI) blend. Polyethylene resin has a melt index of 1.8 dg / min (at 190 ° C / 2.16 kg) and a density of 0.923 g / cm3. The ESI resin used was the INDEX DS 201 brand manufactured by dow Chemical Company using a restricted geometry catalyst. About 70/30 of the styrene / ethylene copolymer resin has a melt index (at 19.0 / 2.16 kg) of 1.1. The foam is prepared from a blend of 70/30 polyethylene resin and ES copolymer resin, and polyethylene. The foam expansion procedure is substantially the same as in Example 1. The foams prepared in this example are listed in Table 10. Isobutane was used in the amount of 9.13 pph as a foaming agent for the preparation of all foams. As in Example 1, a small amount of glycerol-stearic acid was added to control the dimensional stability of the foam. For the preparation of polyethylene foam (PEF6) and ESF1 PE / ESI blend foam 'A small amount of talc was added in a concentrated form (50% of talc in the same polyethylene) for cell size control. The effective talc content of PEF6 foam was 0.068 pph and ESF1 was 0.034 pph. Both ESF 丨 and E.SF2 foams were prepared from the same blend of polyethylene and ESI resin. A small amount (0.05 pph) of an anti-cidal agent (Cerba Geigy Corp.'s Irganox 101) was added to all three foams. Under the cooling zone temperature of about uo ° c and the mold temperature of lire, the three paper sizes are applicable to the Chinese national standard (CNS> A4 specification (210X297 mm) — ^ nf-----1 I— ^^ — ^ 1 —1— ^^^ 1 ^ —I nn Έ-^^^ 1 ^^^ 1n ^ i ml ^^^ 1 (Please read the notes on the back before filling this page) 41 460518-V. Description of the invention ) All formulas are manufactured into foams of excellent quality. The cross-sectional dimensions of the foam are about 60 mm thick and about 620 mm wide. As shown in Table 10, the foam has a density of about 29-30 kg / m3 and a large cell size. The average cell size ranges from 5.6 to 6.7 mm. Table 10 Foam name Foam density (kg / m3) Cell size vertical (mm) Cell size extrusion (mm) Cell size level (mm) Cell size extrusion level average (mm) Cell 3D Average (mm) PEF6 30 7.4 6.0 6.8 6.4 6.7 ESF1 29 5.8 6.0 4.9 5.5 5.6 ESF2 29 6.8 6.8 6.0 6.4 6.5 Note: ()) to (5) = same test as in Table 1 11 Formed by punching and compression The printed consumer body of the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs of the Open Cell was cut into 35mm plates and punched with a 2mm diameter needle at a distance of 10mm and 5mm. A 45 mm diameter cylindrical sample was drilled from the plate. A sample with a 5tnm pore spacing is compressed to 95% of its thickness and further forms an open cell. All the compressed foams returned to their original thickness. The open cell was measured using a 45 mm diameter and 35 mm thick cylindrical sample. The open cell content was determined according to ASTM D-2856 procedure C. As shown in Table 11, the desired high open cell content can be formed by punching. Since the 5mm pitch punch has already provided an open cell content in the range of 92 to 95%, there are fewer open cells that are further formed by compression. As foreseen, ESFs with slightly smaller cells than the others form slightly fewer open cells. This paper size is applicable to China National Standard (CNS) A4 (210X297 mm) 42 460518 A7 B7 V. Description of the invention (4 is called Table 11 Foam name 10mm pitch ⑴ 5mm pitch ⑵ 5mm pitch & compression ⑴ PEF6 72.5 94.7 95.3 ESF1 69.2 92.6 94.5 ESF2 72.9 94.4 95.7 Note: All open cell content is measured in accordance with ASTMD-2856 procedure C (1) Percentage of open cell content of foams perforated at 10mm pitch (2) Perforated hair at 5mm pitch The percentage of the open cell content of the foam (3) is perforated at a pitch of 10mm and then compressed to a percentage of the open content of 95% of the original thickness of the foam. The mechanical and shock-absorbing properties of the cellular foam were determined. The applicability of the foam material as an insert in a sandwich panel was determined. The dynamic stiffness and loss factor were measured using a vibration platform. A diameter of '1 A disk-shaped foam sample with a thickness of 35 cm is mounted on a vibration platform. A circular particle board of the same diameter is loaded on the top of the sample. The surface weight of the particle board is about 10 kg / m3. One accelerometer is attached under the platform and the other accelerometer is attached on the top surface of the particle board load. The platform vibrates at random frequency and the damping ratio is used by the accelerometer signal in a test 4. Brueel and Kjaer model 3 55 5 measured by a signal analyzer. Dynamic stiffness is calculated from the resonance frequency and the loss factor is calculated from the damping ratio. The mechanical and vibration properties of the foam are shown in Table 12. JI1 ---装 ---- install ---,-Ί order ------ free ',. (Please read the notes on the back before filling out this page) gig! Jia Wang ^ (cNS > Eight 4 display_ (2jQx297) -43-A7 B7 5051 8 V. Description of the invention (4 /) Table 12 Foam name Needle pitch (1) Compression strength ⑵ Compression modulus (3) Tensile strength h (4) Tensile modulus (5) Tensile length (6) Dynamic stiffness ⑺ Loss factor PEF6 10 25 747 154 1260 30 3.5 0.43 PEF6 5 22 566 ND ND ND 1.7 035 ESF1 10 17 482 131 790 51 4.8 0.46 ESF1 5 15 362 ND ND ND 3.2 0.48 ESF2 10 16 464 134 814 54 5.0 0.39 ESF2 5 14 332 ND ND ND 3.1 0.46 Printed by the cooperative. Note: ND = to measure (1) the distance between the holes in a square case in millimeters (2) the vertical compressive strength in kilopascals measured in accordance with ASTMD-3575 (3) measured in accordance with ASTM D-3575 Tensile strength in kPa in vertical direction (4) Tensile strength measured in kPa in vertical direction at break in accordance with ASTMD-3 5 7 5 (5) Vertical in kPa measured in accordance with ASTM D-3575 Tensile modulus in direction (6) Tensile length percentage in the vertical direction measured in accordance with ASTM C-3575 (7) Meganewton per cubic meter measured with a 35mm thick foam test piece with a surface weight of 10 per square meter Dynamic stiffness (8) The loss factor measured under the same conditions as the dynamic stiffness is shown in the table. The foam has the appropriate compressive strength and tensile toughness for use as a sandwich panel insert. As expected, blending in the ESI resin made the foam softer. PE / ESI blend foams are stronger by their greater elongation. A higher density punch with a 5mm pitch results in a slight reduction in compressive strength. Higher punching densities have proven to have a greater impact on dynamic stiffness. Advantageously, the dynamic stiffness is reduced to a greater extent than the compressive strength. All foams exhibit good damping characteristics with low loss factors ranging from 0.354 to 0.48. As expected for highly damped ESI resins, PE / ESI blend foams generally have a higher loss factor than PE foams, but the differences between foams with 10 mm pitch cells are small. Interestingly, a favorable increase in a loss factor was observed for PE / ESI blend foams with more punching. Conversely, PE foams experience a reduction in the loss factor when there is a large amount of redemption. This paper size applies to China National Standard (CNS) A4 specification (210X 297 mm) ---------- install ---.-- 1 order ------ 喋---(please first (Read the notes on the back and fill in this page) 44 Printed by the Intellectual Property Bureau of the Ministry of Economic Affairs's Consumer Cooperatives a 605 1 B A7 B7 V. Description of the invention) Test 13 Sound absorption coefficient The sound absorption coefficient of punched giant porous foam is in accordance with ASTM E 1050 is measured using the device described in Test 4. As shown in Table 13, the polymer composition has a slight effect on the sound absorption capacity of the foam. As previously observed, a high pore density deteriorates the sound absorption ability. The good sound absorption performance of a giant multi-cellular foam was confirmed again by punching foams with holes of 10 mm pitch. Table 13 Foam name Pin pitch (1) Sound absorption coefficient 250 Hz (2) 500 Hz (3) 1000 Hz (4) 2000 Hz (5) Maximum (6) Frequency (Hz) (7) PEF6 10 0.21 0.77 0.60 0.75 LOO 800 ESF1 10 0.16 0.79 0.46 0.61 0,92 740 ESF2 10 0.15 0,77 0.50 0,64 0.95 780 PEF6 5 0.08 0.28 0.96 0.43 0,99 960 ESF1 5 0.09 0,29 0.96 0.67 0.98 1020 ESF2 5 0.08 0.25 0 , 96 0.59 0.99 1030, Note: (1) Distance between holes in a square pattern in millimeters (2) Sound absorption coefficient (3) according to ASTM E-1050 at a frequency of 250 Hz according to ASTM E-050 Sound absorption coefficient (4) measured at a frequency of 500 Hz (4) Sound absorption coefficient measured at a frequency of 1000 Hz (5) Sound absorption coefficient measured at a frequency of 2000 Hz according to ASTM E-1050 ( 6) The maximum sound absorption coefficient at frequencies below 1600 Hz (7) The frequency at which the maximum occurs This paper size applies the Chinese National Standard (CNS) A4 specification (210X297 mm) J-1 — Ί ---- Install ---.-- Ί Order ------ 嗲 ·-, (Please read the notes on the back before filling this page) 45 460518 A7 B7, FZ correction year 5. Description of the invention (43) Comparison of component numbers 1 Foam body 2 Closed cell 3 Sharp object 4 Squeeze / press direction 5 Foam core 6 Foam body —, ----.----- ---.Equipment ---- ^ ----- Order --------- line- (Please read the business matters on the back before filling in this page) The paper size of the paper is applicable to China National Standard (CNS) A4 (210 X 297 mm)

Claims (1)

經濟部智慧財產局員工消費合作杜印製 6Π518 asPrinted by the Intellectual Property Bureau of the Ministry of Economic Affairs on Consumer Cooperative Printing 6Π518 as 第088 108888號專利申請案申請專利範圍修正本 修正曰期:90年月 1·一種製備一多孔熱塑性發泡體構造之方法,包括之步驟 a) 提供一具有從2mm至15mm之平均胞室直徑之— 第一多孔熱塑性聚合物發泡體,其中至少某些部分 之胞室為敞開胞室;以及 b) 在該第一熱塑性聚合物發泡體構造之至少一表面 的至少某些部分運用一敞開一多孔熱塑性聚合物 發泡體中之閉合胞室的手段,此一運用係足以生成 一具有自2mm至15mm之平均胞室直徑的多孔熱 塑性聚合物發泡體構造’其中大於5〇百分比之胞 室已藉運用該敞開一多孔熱塑性聚合物發泡體内 之閉合胞室的手段被敞開,其中該敞開胞室百分含 量係依據ASTM D-28.56,程序C來測量。 2. 如申請專利範圍第1項之方法,其中該第一多孔熱塑性 聚合物發泡趙構造係實質上閉合胞室者。 3. 如申請專利範圍第1項之方法’其中該第一多孔熱塑性 聚合物發泡體構造係實質上敞開胞室者。 4. 如申請專利範圍第1項之方法,其中該第一多孔熱塑性 聚合物發泡體構造具有一為2mm至10mm之平均胞室 直徑》 5. 如申請專利範圍第4項之方法,其中該第一多孔熱塑性 聚合物發泡艘構造具有一為3 mm至10mm之平均胞室 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐〉 --- Is— ----I----衣' —-------訂·--------. (请先Μ讀背面之注意事項再填寫本頁)No. 088 108888 Patent Application Amendment to Patent Scope Amendment Date: January 1990 1. A method of preparing a porous thermoplastic foam structure, including the step a) providing an average cell with a cell diameter from 2mm to 15mm Of diameter—the first porous thermoplastic polymer foam, wherein at least some portions of the cells are open cells; and b) at least some portions of at least one surface of the first thermoplastic polymer foam structure By means of opening a closed cell in a porous thermoplastic polymer foam, this application is sufficient to produce a porous thermoplastic polymer foam structure having an average cell diameter from 2mm to 15mm, where more than 5 The percentage of cells has been opened by using the method of opening the closed cells of a porous thermoplastic polymer foam, wherein the percentage of open cells is measured according to ASTM D-28.56, procedure C. 2. The method according to item 1 of the patent application scope, wherein the first porous thermoplastic polymer foamed structure is substantially closed cells. 3. The method according to item 1 of the scope of the patent application, wherein the first porous thermoplastic polymer foam structure is substantially open-celled. 4. The method according to item 1 of the patent application, wherein the first porous thermoplastic polymer foam structure has an average cell diameter of 2 mm to 10 mm. 5. The method according to item 4 of the patent application, wherein The first porous thermoplastic polymer foaming vessel structure has an average cell of 3 mm to 10 mm. The paper size is applicable to China National Standard (CNS) A4 (210 X 297 mm) --- Is---- -I ---- 衣 '—------- Order · --------. (Please read the notes on the back before filling in this page) 六、申請專利範圍 η 6〇 51 8 直徑。 6.如申明專利範圍第5項之方法,其中該第一多孔熱塑性 聚合物發泡體構造具有一為4mm至8mm之平均胞室直 徑。 7-如申請專利範圍第!項之方法,其令該第一多孔熱塑性 聚合物發泡體構造係由—稀烴聚合物製備。 8·如申4專利範圍第7項之方法’其中該稀烴聚合物係擇 自於烯屬聚合物、共聚物或其等之摻合物。 9.如申請專利範圍第7項之方法,其中該稀煙聚合物為聚 丙稀。 如申請專利範圍第7項之方法,其中該烯烴聚合物係為 一聚丙烯和一乙烯-苯乙烯之摻合物。 11. 如申請專利範圍第8項之方法,其中該烯屬聚合物係一 低密度聚乙稀》 12. 如申請專利範圍第8項之方法,其中該烯屬聚合物為一 低密度聚乙烯和一乙烯·笨乙烯共聚體之摻合物。 13. 如申請專利範圍第12項之方法,其中該乙烯笨乙烯共 5«體具有一以重量計為至少6〇%之苯乙烯含量a 14. 如申請專利範圍第12項之方法,其中該一低密度聚乙 烯和一乙烯-苯乙烯共聚體之摻合物含有以重量計為至 少50%之低密度聚乙烯。 15·如申請專利範圍第1項之方法,其中高於7〇%之多孔 熱塑性聚合物發泡艘之胞室已經藉由應用—敞開—多 孔熱塑性聚合物發泡體之閉合胞室的手段而敵開。 _______ -2- ϋ張尺度適用t國國家標準(CNS)A4規格C 297公爱)· -___ -IJI IJI — — —--I ^--— — rill·— r I I I I If I - (請先閲讀背面之注意事項再填寫本頁> 經濟部智慧財產局員工消費合作社印製 經濟部智慧財產局員工消費合作社印製 Α8 Β8 CS D8 六、申請專利範圍 1 6_如申請專利範圍第1項之方法,其中高於9〇%之多孔 熱塑性聚合物發泡體之胞室已經藉由應用一敞開一多 孔熱塑性聚合物發泡體之閉合胞室的手段而敞開。 17_如申請專利範圍第1項之方法,其中該多孔熱塑性聚合 物發泡體構造具有一低於80〇,〇〇〇 Rayis/ m之氣流阻 力。 18.如申請專利範圍第17項之方法,其中該多孔熱塑性聚 合物發泡體構造具有一低於40〇,〇〇〇 Rayis/m之氣流 阻力。 Ϊ9.如申請專利範圍第18項之方法,其中該多孔熱塑性聚 合物發泡體構造具有一低於100,000 Rayls/m之氣流 阻力。 20‘如申請專利範圍第19項之方法,其中該多孔熱塑性聚 合物發泡體構造具有一低於5〇,〇〇〇 Rayis/m之氣流阻 力。 21,如申請專利範圍第1項之方法,其中該敞開手段係擇自 於穿孔、切割 '壓縮或其等之組合。 22. 如申請專利範圍第21項之方法,其中該敞開手段包括 切割β 23. 如申請專利範圍第2 1項之方法,其中該敞開手段包括 壓縮。 24. 如申請專利範圍第23項之方法’其中該敞開手段為穿 孔接著壓縮。 25. 如申請專利範圍第21項之方法,其中該敞開手段包括 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公着〉 I I t€ Hi n tsv ti- n u I- (靖先《讀背面之注意事項再填寫本頁) 訂---------線 ASB8C8D8 六 經濟部智慧財產局員工消費合作杜印製 Δ 60518 申請專利範圍 穿孔。 26. 如申請專利範圍第25項之方法,其中該穿孔包括一或 多個正方形圖案。 27. 如申請專利範圍第25項之方法,其中該穿孔包括一或 多個三角形圖案。 28_如申請專利範圍第25項之方法,其中該敞開手段係一 壓縮並接著穿孔。 29 ·如申請專利範圍第25項之方法,其中該穿孔係以一會 造成孔彼此間係以一距離間隔開之方式實施,該距離不 大於該第一多孔熱塑性聚合物發泡體構造中之胞室平 均直徑的兩倍a 30. 如申請專利範圍第29項之方法,其中該穿孔係以一會 造成孔彼此間係以一距離間隔開之方式實施,其中該距 離不大於該第一多孔熱塑性聚合物發泡體構造中之胞 室平均直徑的1.5倍》 31. 如申清專利範圍第30項之方法’其中該穿孔係以一會 造成孔彼此間係以一距離間隔開之方式實施,其中該距 離約等於該第一多孔熱塑性聚合物發泡體構造中之胞 室平均直徑。 32. 如申請專利範圍第30項之方法,其中該穿孔係以一會 造成孔彼此間係以一距離間隔開之方式實施,其中該距 離小於該第一多孔熱塑性聚合物發泡體構造令之胞室 平均直徑。 33. 如申請專利範圍第25項之方法,其中該穿孔包括以一 本紙張尺度適用中國國家標準(CNS>A4規格(210 * 297公釐) « ^1- ^^1 n i s-> at· T— 訂---------線 _ (請先閲讀背面之注意事項再填寫本頁) 8800^9 ABC0 S0518 六、申請專利範圍 或多種尖頭、銳利物體刺穿該第一多孔熱塑性聚合物發 泡趙。 34. 如申請專利範圍第33項之方法,其中該尖頭、銳利物 體擇自於針、銷、刺針或釘。 35. 如申請專利範圍第32項之方法,丨中該穿孔包括以鑽 孔、雷射切割、高壓流體切割、氣搶,或彈丸刺穿該第 一多孔熱塑性聚合物發泡體。 36. 如申請專利範圍第丨項之方法,其中該發泡體進一步包 括一阻燃劑》 37. 如申請專利範圍第丨項之方法,其中該發泡體已被成型 成一具有低動態剛性度之縱剖面a 38. 如申請專利範圍第37項之方法(其中該縱剖面係由多 孔熱塑性發泡體之核心所組成,,該發泡體核心之相對 兩側已任擇地附著相同或一不同於多扎熱塑性聚合物 發泡體窄條。 39. 如申請專利範圍第38項之方法,其中該多孔熱塑性聚 合物發泡體窄條之中點間距離至少為25〇mm β 40. 如申請專利範圍第39項之方法,其中在發泡體同側之 多孔熱塑性聚合物發泡體窄條之中點間距離為3〇〇mm 至 600mm。 41. 如申請專利範圍第37項之方法’其中該縱剖面係由— 多孔熱塑性發泡體核心所組成,該發泡體核心之同一側 及相對兩端已附著相同或一不同於多孔熱塑性聚合物 發泡艘窄條。 本紙張尺度適用中圉國家標準(CNS)A4規格(21Q X 297公g ) I fs J 1 ---nil—^--In.----- - --------I (請先Μ讀背面之江意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印*'Λ 8 i— 5 ο ABCS 六 __ 經濟部智慧財產局員工消費合作社印製 申請專利範圍 42. 如申清專利範圍第41項之方法’其中該窄條之中點間 距離為至少350mm。 43. 如申請專利範圍第42項之方法,其中該窄條之中點間 距離為450mm至600mm 6 44. 如申請專利範圍第1項之方法’其中該敵開手段之應 用僅部分伸展通過該發泡體構造之厚度。 45. —種多孔熱塑性發泡體,其可由如上述申請專利範圍 中任一項之方法獲得。 46· —種適合用於如申請專利範圍第丨·42項中任一項之 方法之發泡體’該發泡體包含一具有一平均胞室直徑 大於4 mm’可藉由將一可發泡之凝膠擠經一多口型模 具至一具較低壓力之區域而得之多孔熱塑性發泡 體’該較低壓力係於一大氣壓下或低於一大氣壓下, 而該可發泡凝膝包含具有混合與一吹融劑之該熱塑 性聚合物。 47. —種適合用於如申請專利範圍第1-42項中任一項之 方法之發泡體,該發泡艘包含一具有一平均胞室直經 大於4 mm之經擠出的多孔熱塑性發泡體,其中該胞室 係被拉長的以及該腔室拉長的方位係該擠出之方向。 48. —種適合用於如申請專利範圍第1-42項中任一項之 方法之發泡艘,該發泡體包含一具有一平均胞室直徑 大於4 mm,且呈結合多股型式之多孔熱塑性發泡趙。 49. 一種適合用於如申請專利範圍第1-42項中任一項之 方法之發泡體,該發泡體包含一具有一平均胞室直徑 本紙張尺度通用令國國家標準(CNS)A4規格(210 X 297公釐) ------------ 我·!-----訂 ------ _線 ·"請先閲讀背面之注意事項再填寫本頁) Λ 6051 8 A8B8C8D8 六、申請專利範圍 大於4 mm ’且呈非交聯珠粒型式之多孔熱塑性發泡體》 50. —種適合用於如申請專利範圍第1_42項中任一項之 方法之發泡體’其中該發泡體係一具有一平均胞室直 徑大於4 mm,且由一已經與一烯基官能矽烷或一疊氮 基官能矽烷接枝之聚合物製成之多孔性聚合物。 51. —種適合用於如申請專利範圍第1-42項中任一項之 方法之發泡體,其中該發泡體係具有一平均胞室直徑 大於4 mm之經交聯的多孔性聚合物發泡艘。 <請先Μ讀背面之注意事項再填Κ本頁) 疚----„---Γ訂---------線 經濟部智慧財產局員工消费合作社印製 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐)6. Scope of patent application η 6〇 51 8 diameter. 6. The method according to claim 5, wherein the first porous thermoplastic polymer foam structure has an average cell diameter of 4 mm to 8 mm. 7- If the scope of patent application is the first! In the method of claim 1, the first porous thermoplastic polymer foam structure is prepared from a dilute hydrocarbon polymer. 8. The method of item 7 in the scope of the patent of claim 4, wherein the dilute hydrocarbon polymer is selected from an olefinic polymer, a copolymer, or a blend thereof. 9. The method of claim 7 in the scope of patent application, wherein the thin smoke polymer is polypropylene. The method of claim 7 in which the olefin polymer is a blend of a polypropylene and an ethylene-styrene. 11. The method according to item 8 of the patent application, wherein the olefinic polymer is a low density polyethylene "12. The method according to item 8 of the patent application, wherein the olefinic polymer is a low density polyethylene Blends with monoethylene · stupene copolymers. 13. The method according to item 12 of the patent application, wherein the total amount of ethylene styrene has a styrene content of at least 60% by weight a 14. The method according to item 12 of the patent application, wherein the A blend of a low density polyethylene and an ethylene-styrene interpolymer contains at least 50% by weight of low density polyethylene. 15. The method according to item 1 of the patent application range, in which more than 70% of the cells of the porous thermoplastic polymer foaming vessel have been applied by means of-opening-the closed cells of the porous thermoplastic polymer foam The enemy opened. _______ -2- Applicable to national standards (CNS) A4 specifications C 297 public love)----IJI IJI — — — --I ^-— — rill · — r IIII If I-(Please first Read the notes on the back and fill out this page> Printed by the Employees 'Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs Printed by the Employees' Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs Printed by A8 Β8 CS D8 In this method, the cells of more than 90% of the porous thermoplastic polymer foam have been opened by applying a method of opening the closed cells of a porous thermoplastic polymer foam. The method according to item 1, wherein the porous thermoplastic polymer foam structure has an airflow resistance of less than 80,000 Rayis / m. 18. The method according to item 17 of the patent application scope, wherein the porous thermoplastic polymer The foam structure has an airflow resistance of less than 40,000 Rayis / m. Ϊ9. The method according to item 18 of the patent application scope, wherein the porous thermoplastic polymer foam structure has a value of less than 100,000 Rayls / m of airflow resistance 20 'The method according to item 19 in the scope of patent application, wherein the porous thermoplastic polymer foam structure has an airflow resistance of less than 50,000 Rayis / m. 21, as in the first item in scope of patent application Method, wherein the open means is selected from the group consisting of perforation, cutting, compression, or the like. 22. The method of applying the scope of patent No. 21, wherein the open means includes cutting beta 23. Such as the scope of applying patent No. 21 Method, wherein the means for opening includes compression. 24. The method for applying scope of patent No. 23, wherein the method for opening is perforation followed by compression. 25. The method for applying scope, including the paper, includes the paper The scale is applicable to the Chinese National Standard (CNS) A4 specification (210 X 297)> II t € Hi n tsv ti- nu I- (Jing Xian "Read the precautions on the back before filling this page) Order ------- --Line ASB8C8D8 The consumer cooperation of the Intellectual Property Bureau of the Ministry of Economic Affairs of the People's Republic of China printed 6060518 patent application perforation. 26. For the method of applying for patent scope item 25, wherein the perforation includes one or more square patterns 27. If the method of applying for the scope of the patent item 25, wherein the perforation comprises one or more triangular patterns. 28_If the method of applying for the scope of the patent item 25, wherein the opening means is a compression and then perforation. 29 · Such as The method of claim 25, wherein the perforation is implemented in such a manner that the pores are spaced apart from each other by a distance that is not greater than the cell in the first porous thermoplastic polymer foam structure. The average diameter is twice a 30. The method according to item 29 of the patent application, wherein the perforation is performed in such a manner that the pores are spaced apart from each other by a distance, wherein the distance is not greater than the first porous thermoplastic 1.5 times the average cell diameter in the polymer foam structure "31. The method of claim 30 of the patent scope 'where the perforations are implemented in such a way that the holes are spaced apart from each other by a distance, The distance is approximately equal to the average cell diameter in the first porous thermoplastic polymer foam structure. 32. The method of claim 30, wherein the perforation is implemented in such a manner that the holes are spaced apart from each other by a distance, wherein the distance is less than the first porous thermoplastic polymer foam structure order Cell cell average diameter. 33. The method of claim 25, wherein the perforation includes applying a Chinese paper standard (CNS > A4 specification (210 * 297 mm) at a paper size) «^ 1- ^^ 1 ni s- > at · T—Order --------- Line_ (Please read the precautions on the back before filling in this page) 8800 ^ 9 ABC0 S0518 6. Application scope of patent or multiple pointed or sharp objects piercing the first Porous thermoplastic polymer foam Zhao. 34. If the method of the scope of the patent application No. 33, wherein the pointed, sharp object is selected from a needle, pin, puncture needle or nail. 35. If the method of the scope of patent application 32 The perforation includes drilling, laser cutting, high-pressure fluid cutting, gas grabbing, or projectile piercing the first porous thermoplastic polymer foam. 36. The method according to item 丨 of the patent application, wherein The foam further includes a flame retardant "37. The method according to item 丨 of the scope of patent application, wherein the foam has been formed into a longitudinal section with low dynamic rigidity a 38. The item under scope of patent application 37 Method (where the longitudinal section is made of porous thermoplastic foam Composed of the core of the body, the opposite sides of the core of the foam have optionally been attached with the same or a narrow strip of thermoplastic polymer foam different from Doza. 39. For example, the method of claim 38 in the scope of patent application, wherein The distance between the middle points of the narrow strips of the porous thermoplastic polymer foam is at least 25 mm β 40. The method according to item 39 of the patent application, wherein the narrow strips of the porous thermoplastic polymer foam on the same side of the foam The distance between the midpoints is 300mm to 600mm. 41. The method of the 37th aspect of the patent application 'where the longitudinal section is composed of-a porous thermoplastic foam core, the same side of the foam core and The opposite ends have been attached with the same or a narrow strip different from the porous thermoplastic polymer foaming vessel. This paper size applies to the China National Standard (CNS) A4 specification (21Q X 297 g) I fs J 1 --- nil— ^ --In .-------------- I (Please read the Jiang Yi matters on the back before filling out this page) Seal of Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs * 'Λ 8 i— 5 ο ABCS VI __ Intellectual Property Bureau of the Ministry of Economic Affairs printed the scope of patent application for consumer cooperatives 42. Such as Method for claiming item 41 of the patent scope 'wherein the distance between the middle points of the narrow strip is at least 350mm. 43. As for the method of applying item 42 of the patent scope, wherein the distance between the middle points of the narrow strip is 450mm to 600mm 6 44 The method according to item 1 of the scope of patent application 'where the application of the enemy means only partially extends through the thickness of the foam structure. 45.-A porous thermoplastic foam, which can be used by any of the scope of the above patent application Item. 46 · —A foam suitable for use in a method according to any one of the scope of the patent application No. 丨 · 42, the foam includes a foam having an average cell diameter greater than 4 mm. A porous thermoplastic foam obtained by extruding a foamed gel through a multi-port die to a region with a lower pressure. The lower pressure is at or below atmospheric pressure, and the foamable gel The knee contains the thermoplastic polymer with a blend and a blowing agent. 47. A foam suitable for use in a method according to any of claims 1-42 of the patent application scope, the foam vessel comprising an extruded porous thermoplastic having an average cell straight through greater than 4 mm The foam, wherein the cell line is elongated and the cavity elongated orientation is the direction of the extrusion. 48. A foaming vessel suitable for use in a method according to any of claims 1-42 of the scope of patent application, the foaming body comprises a foamed vessel having an average cell diameter greater than 4 mm, and a combination of multiple strands Porous thermoplastic foam Zhao. 49. A foam suitable for use in a method according to any of claims 1-42 of the scope of patent application, the foam comprising an average cell diameter, a paper standard, and Common National Standard (CNS) A4 Specifications (210 X 297 mm) ------------ I ·! ----- Order ------ _Line · " Please read the precautions on the back before filling in this page) Λ 6051 8 A8B8C8D8 6. Apply for a patent scope greater than 4 mm 'and present a non-crosslinked bead type "Porous thermoplastic foam" 50. —A foam suitable for use in a method according to any one of the scope of patent applications No. 1-42 'wherein the foam system has an average cell diameter greater than 4 mm, and A porous polymer that has been grafted with an alkenyl-functional silane or an azide-functional silane. 51. A foam suitable for use in a method according to any one of claims 1-42, wherein the foam system has a crosslinked porous polymer having an average cell diameter greater than 4 mm Foaming ship. < Please read the precautions on the back before filling in this page) Guilt ---- --------- Order --------- Printed on paper by the Consumers ’Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs Applicable to China National Standard (CNS) A4 (210 X 297 mm)
TW088108888A 1998-09-17 1999-05-28 Preparing process of cellular thermoplastic polymer foam and manufactured products thereof, and foam suitable for use therein TW460518B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US10069998P 1998-09-17 1998-09-17

Publications (1)

Publication Number Publication Date
TW460518B true TW460518B (en) 2001-10-21

Family

ID=22281093

Family Applications (1)

Application Number Title Priority Date Filing Date
TW088108888A TW460518B (en) 1998-09-17 1999-05-28 Preparing process of cellular thermoplastic polymer foam and manufactured products thereof, and foam suitable for use therein

Country Status (19)

Country Link
EP (1) EP1115777B1 (en)
JP (1) JP2002524635A (en)
KR (1) KR100588251B1 (en)
CN (1) CN1232572C (en)
AT (1) ATE221097T1 (en)
AU (1) AU768157B2 (en)
BR (1) BR9913966A (en)
CA (1) CA2340217C (en)
CZ (1) CZ2001563A3 (en)
DE (1) DE69902283T2 (en)
DK (1) DK1115777T3 (en)
ES (1) ES2177280T3 (en)
HU (1) HUP0103869A3 (en)
IL (1) IL141518A0 (en)
NO (1) NO20011347L (en)
TR (1) TR200100743T2 (en)
TW (1) TW460518B (en)
WO (1) WO2000015697A1 (en)
ZA (2) ZA200101148B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI619603B (en) * 2016-08-26 2018-04-01 黃淑娟 Acoustic absorber, producing method thereof and tooling thereof

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19962865C1 (en) * 1999-12-24 2001-02-15 Bayer Ag Shaped polymer foam component for sound absorption purposes in automobiles is provided with perforations in its compacted surface layer
US6649671B2 (en) * 2000-03-13 2003-11-18 Dow Global Technologies Inc. Concrete and process to make same
EP1268155B1 (en) * 2000-03-17 2005-04-06 Dow Global Technologies Inc. Acoustic absorption polymer foam having improved thermal insulating performance
CN100432127C (en) 2000-03-17 2008-11-12 陶氏环球技术公司 Prepn. of macrocellular acoustic foam
US20020153199A1 (en) * 2001-02-09 2002-10-24 Schroer Daniel R. Sound absorbing foam
ES2314186T3 (en) 2002-02-22 2009-03-16 Dow Global Technologies Inc. THERMOPLASTIC FOAM CONTAINING ADDITIVE IN THE FORM OF PARTICLES.
US6770683B2 (en) 2002-02-22 2004-08-03 Sealed Air Corporation (Us) Foam comprising a blend of ethylene/styrene interpolymer and polyethylene
DE10212729B4 (en) * 2002-03-22 2010-03-04 Gefinex Gesellschaft für innovative Extrusionsprodukte mbH Polyethylene foams with low dynamic stiffness
US7144925B2 (en) 2002-05-09 2006-12-05 Dow Global Technologies Inc. Fire resistance acoustic foam
US20030225172A1 (en) * 2002-05-31 2003-12-04 Miller Larry M. To enhance the thermal insulation of polymeric foam by reducing cell anisotropic ratio and the method for production thereof
US20030228458A1 (en) * 2002-06-11 2003-12-11 Mario Lorini Perforated closed-cell foamed material and method for manufacture
KR20080114840A (en) * 2003-07-16 2008-12-31 세키스이가가쿠 고교가부시키가이샤 Foam sheet of crosslinked polyolefin resin, process for producing the same, and pressure-sensitive adhesive tape
JP4187101B2 (en) * 2003-08-01 2008-11-26 河西工業株式会社 Sound absorbing material for vehicle and method for manufacturing the same
TW200517426A (en) * 2003-08-25 2005-06-01 Dow Global Technologies Inc Aqueous dispersion, its production method, and its use
CN100346955C (en) * 2003-09-01 2007-11-07 刘坤钟 Manufacturing method of porous elastic foamed body and its equipment
WO2005073299A1 (en) * 2004-01-28 2005-08-11 Sekisui Chemical Co., Ltd. Thermoplastic resin foam sheet and method for producing thermoplastic resin foam sheet
DE102004042297A1 (en) * 2004-09-01 2006-03-02 Trocellen Gmbh Open-cell and cross-linked polymer foam made of polyolefins and polystyrene
US7968180B2 (en) 2005-04-27 2011-06-28 Prime Polymer Co., Ltd. Extruded propylene-resin composite foam
US8158689B2 (en) 2005-12-22 2012-04-17 Kimberly-Clark Worldwide, Inc. Hybrid absorbent foam and articles containing it
EP1820818A1 (en) 2006-02-15 2007-08-22 Trocellen GmbH Process for manufacturing an open celled and cross-linked polyolefine foam
RU2010151144A (en) * 2008-05-16 2012-06-27 ПРОПРИТЕКТ ЭлЭлПи (CA) FOAMED LAYERED PRODUCT AND METHOD FOR ITS MANUFACTURE
KR101331665B1 (en) * 2008-12-04 2013-11-20 (주)엘지하우시스 Method of manufacturing Interfloor noise proofing material
DE102009028200A1 (en) 2009-08-04 2011-02-17 Evonik Degussa Gmbh Use of amorphous polyolefin to produce foam, where used polyolefin exhibits three of following conditions specified range of melting enthalpy, softening point, needle penetration, tensile strength and glass transition temperature
JP5643018B2 (en) * 2010-07-27 2014-12-17 Dmノバフォーム株式会社 Foam, production method thereof and use thereof
JP5626995B2 (en) * 2011-02-15 2014-11-19 株式会社神戸製鋼所 Sound absorption panel
EP2524788A1 (en) 2011-05-16 2012-11-21 Sealed Air Corporation (US) Method of perforating a foam structure and an acoustic foam structure
CN102320138A (en) * 2011-09-10 2012-01-18 无锡吉兴汽车声学部件科技有限公司 Manufacturing method of ultra-mute car ceiling
AU2013215067A1 (en) * 2012-02-02 2014-06-12 Kci Licensing, Inc. Foam structure wound inserts for directional granulation
US20170305209A1 (en) * 2014-10-03 2017-10-26 Pirelli Tyre S.P.A. Soundproof tyre for vehicle wheels
JP6566200B2 (en) * 2015-07-23 2019-08-28 キョーラク株式会社 Foam
WO2017163219A1 (en) * 2016-03-25 2017-09-28 Pirelli Tyre S.P.A. Soundproof self-sealing tyre for vehicle wheels
CN106221603A (en) * 2016-09-20 2016-12-14 东莞市纳利光学材料有限公司 A kind of noise reduction protecting film and preparation method thereof
EP3565514A1 (en) * 2017-01-09 2019-11-13 KCI Licensing, Inc. Wound dressing layer for improved fluid removal
JP7189059B2 (en) * 2019-03-27 2022-12-13 積水化成品工業株式会社 Foamed sheet and method for manufacturing foamed sheet
CN111376503B (en) * 2020-02-24 2021-09-28 中国科学院宁波材料技术与工程研究所 Method for accelerating volume recovery of elastomer foam material
WO2022013421A1 (en) 2020-07-17 2022-01-20 Recticel Noise barrier and apparatus comprising the noise barrier
CN112280184A (en) * 2020-11-10 2021-01-29 中嘉卫华(固安)新材料科技有限公司 Electron irradiation crosslinking foaming polypropylene heat preservation belt and preparation method thereof
KR102710555B1 (en) * 2023-04-25 2024-09-27 프라임에너텍㈜ Semi-non combustible foam materials, insulation sheets and building materials

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4154785A (en) * 1974-10-22 1979-05-15 The Furukawa Electric Co., Ltd. Method of manufacturing a tough board of thermoplastic resin foam having integral skins and a dense intermediate layer
EP0602262B1 (en) * 1992-12-15 1997-03-12 Scriptoria N.V. Continuous polyolefin foam panels

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI619603B (en) * 2016-08-26 2018-04-01 黃淑娟 Acoustic absorber, producing method thereof and tooling thereof

Also Published As

Publication number Publication date
AU768157B2 (en) 2003-12-04
JP2002524635A (en) 2002-08-06
EP1115777B1 (en) 2002-07-24
DE69902283D1 (en) 2002-08-29
CA2340217C (en) 2009-10-06
HUP0103869A3 (en) 2003-05-28
HUP0103869A2 (en) 2002-02-28
ATE221097T1 (en) 2002-08-15
IL141518A0 (en) 2002-03-10
NO20011347D0 (en) 2001-03-16
AU4212499A (en) 2000-04-03
DK1115777T3 (en) 2002-11-18
ZA200101289B (en) 2001-08-21
KR20010075181A (en) 2001-08-09
CN1318078A (en) 2001-10-17
EP1115777A1 (en) 2001-07-18
WO2000015697A1 (en) 2000-03-23
CA2340217A1 (en) 2000-03-23
CN1232572C (en) 2005-12-21
TR200100743T2 (en) 2001-06-21
CZ2001563A3 (en) 2001-11-14
ZA200101148B (en) 2001-09-18
BR9913966A (en) 2001-07-03
KR100588251B1 (en) 2006-06-12
NO20011347L (en) 2001-05-03
ES2177280T3 (en) 2002-12-01
DE69902283T2 (en) 2003-03-13

Similar Documents

Publication Publication Date Title
TW460518B (en) Preparing process of cellular thermoplastic polymer foam and manufactured products thereof, and foam suitable for use therein
US6720362B1 (en) Perforated foams
KR100686487B1 (en) An acoustic absorption polymer foam having improved thermal insulating performance and a process for preparing the same
US5770634A (en) Foam materials for insulation, derived from high internal phase emulsions
RU2205754C2 (en) Multilayer foam plastics
US6071580A (en) Absorbent, extruded thermoplastic foams
US9056961B2 (en) Melamine-resin foams comprising hollow microbeads
KR100253968B1 (en) Use of foam materials derived from high internal phase emulsions for insulation
US6454981B1 (en) Method of forming a partially perforated foam
JP2001353763A (en) Polyolefin resin open cell foam extrusion foamed sheet
MXPA01002803A (en) Perforated foams
JPH07268983A (en) Wall heat insulating material for wooden framework building
JPH07217014A (en) Floor heat insulating material for wooden building
JPH07292797A (en) Spacer integral type heat shielding member
JPH0362543B2 (en)
JPH07224470A (en) Heat insulating material for wall of wood framing building

Legal Events

Date Code Title Description
GD4A Issue of patent certificate for granted invention patent
MM4A Annulment or lapse of patent due to non-payment of fees